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
C/G|Ancestral: C|Ambiguity code: S
Location

This variant maps to 3 genomic locations; None selected

Evidence status

Synonyms

Archive dbSNP rs3200251, rs17211064

HGVS name

None

About this variant

This variant overlaps 1 regulatory feature and has 28 sample genotypes.

Variant displays