rs12243326

Associated Genes

Type

Snp

Classification

Not Available

Locations

AssemblySequencePositionAllelesSource
GRCh38NC_000010.11(opens in new window)113029056
  • T > C
dbSnp
GRCh37NC_000010.10(opens in new window)114788815
  • T > C
dbSnp
NG_012631.1(opens in new window)83807
  • T > C
dbSnp

Variant Frequencies

Identifiers

PharmGKB ID

PA166154144

Aliases

  • rs17685444 (retired)
  • rs60689663 (retired)
  • NC_000010.10:g.114788815T>C
  • NC_000010.11:g.113029056T>C
  • NG_012631.1:g.83807T>C
  • NM_001146274.1:c.451-10969T>C
  • NM_001146283.1:c.382-10969T>C
  • NM_001146284.1:c.382-10969T>C
  • NM_001146285.1:c.382-10969T>C
  • NM_001146286.1:c.382-10969T>C
  • NM_001198525.1:c.382-10969T>C
  • NM_001198526.1:c.382-10969T>C
  • NM_001198527.1:c.382-10969T>C
  • NM_001198528.1:c.382-10969T>C
  • NM_001198529.1:c.382-10969T>C
  • NM_001198530.1:c.381+77449T>C
  • NM_001198531.1:c.451-10969T>C
  • NM_030756.4:c.382-10969T>C
  • XM_005270071.1:c.451-10969T>C
  • XM_005270072.1:c.451-10969T>C
  • XM_005270073.1:c.451-10969T>C
  • XM_005270074.1:c.451-10969T>C
  • XM_005270075.1:c.451-10969T>C
  • XM_005270076.1:c.451-10969T>C
  • XM_005270077.1:c.451-10969T>C
  • XM_005270078.1:c.451-10969T>C
  • XM_005270079.1:c.451-10969T>C
  • XM_005270080.1:c.382-10969T>C
  • XM_005270081.1:c.382-10969T>C
  • XM_005270082.1:c.451-10969T>C
  • XM_005270083.1:c.451-10969T>C
  • XM_005270084.1:c.451-10969T>C
  • XM_005270085.1:c.451-10969T>C
  • XM_005270086.1:c.382-10969T>C
  • XM_005270087.1:c.382-10969T>C
  • XM_005270088.1:c.382-10969T>C
  • XM_005270089.1:c.382-10969T>C
  • XM_005270090.1:c.381+77449T>C
  • XM_005270091.1:c.451-10969T>C
  • XM_005270091.2:c.451-10969T>C
  • XM_005270092.1:c.451-10969T>C
  • XM_005270093.1:c.451-10969T>C
  • XM_005270094.1:c.451-10969T>C
  • XM_005270095.1:c.451-10969T>C
  • XM_005270096.1:c.451-10969T>C
  • XM_005270100.1:c.451-10969T>C
  • XM_005270101.1:c.382-10969T>C
  • XM_005270102.1:c.451-10969T>C
  • XM_005270103.1:c.382-10969T>C
  • XM_005270104.1:c.382-10969T>C
  • XM_006717956.2:c.-9-10969T>C
  • XM_011540109.1:c.451-10969T>C
  • XM_011540110.1:c.382-10969T>C
  • XM_011540111.1:c.382-10969T>C
  • XM_011540112.1:c.451-10969T>C
  • XM_011540113.1:c.451-10969T>C
  • XM_011540114.1:c.451-10969T>C
  • XM_011540115.1:c.451-10969T>C
  • XM_011540116.1:c.451-10969T>C
  • XM_011540117.1:c.451-10969T>C
  • XM_011540118.1:c.451-10969T>C
  • XM_011540119.1:c.451-10969T>C
  • rs17685444
  • rs60689663

History

No history available.