This variant maps to 2 locations

Select a location:
Original source

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

Alleles
C/G|Ancestral: C|Ambiguity code: S|MAF: 0.29 (G)
Location

This variant maps to 2 genomic locations; None selected

Evidence status

Synonyms

Archive dbSNP rs386506072, rs17305297

HGVS name

None

About this variant

This variant overlaps 1 regulatory feature and has 3116 sample genotypes.

Variant displays