This variant maps to 3 locations

Select a location:
Original source

Variants (including SNPs and indels) imported from dbSNP (release 144)|View in dbSNP

Alleles
T/A/G|Ancestral: T|Ambiguity code: D
Location

This variant maps to 3 genomic locations; None selected

Evidence status

Synonyms

Archive dbSNP rs3816985, rs34274884

HGVS name

None

About this variant

This variant is mentioned in 1 citation.

Variant displays