rs34898711

Associated Genes

Type

Multinucleotide variation

Classification

Intronic

Locations

AssemblySequencePositionAllelesSource
GRCh38NC_000022.11(opens in new window)42131066 - 42131067
  • GG > AA
dbSnp
GRCh37NC_000022.10(opens in new window)42527068 - 42527069
  • GG > AA
dbSnp
NG_008376.3(opens in new window)3925 - 3926
  • CC > TT
dbSnp
NG_008376.4(opens in new window)4744 - 4745
  • CC > TT
dbSnp
NG_055460.1(opens in new window)351 - 352
  • GG > AA
dbSnp

Variant Frequencies

Identifiers

PharmGKB ID

PA166178865

Aliases

    History

    No history available.