rs17731538

Associated Genes

Type

Snp

Classification

Intronic

Locations

AssemblySequencePositionAllelesSource
GRCh38NC_000004.12(opens in new window)88134227
  • G > A
dbSnp
GRCh37NC_000004.11(opens in new window)89055379
  • G > A
dbSnp
NG_032067.2(opens in new window)102096
  • C > T
dbSnp

Variant Frequencies

Identifiers

PharmGKB ID

PA166156674

Aliases

  • rs57419238 (retired)
  • NC_000004.11:g.89055379G>A
  • NC_000004.12:g.88134227G>A
  • NG_032067.2:g.102096C>T
  • NM_001257386.1:c.204-1592C>T
  • NM_004827.2:c.204-1592C>T
  • XM_005263354.1:c.204-1592C>T
  • XM_005263354.2:c.204-1592C>T
  • XM_005263355.1:c.204-1592C>T
  • XM_005263355.2:c.204-1592C>T
  • XM_005263356.1:c.204-1592C>T
  • XM_005263356.2:c.204-1592C>T
  • XM_011532420.1:c.204-1592C>T
  • rs57419238

History

No history available.