This variant maps to 7 locations

Select a location:
Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | View in dbSNP

Alleles
C/A | Ancestral: C | Ambiguity code: M | MAF: 0.15 (A)
Location

This variant maps to 7 genomic locations; None selected

Evidence status

HGVS name

None

This variant has assays on 8 chips - click the plus to show

About this variant

This variant overlaps 1 regulatory feature, has 2505 sample genotypes and is mentioned in 86 citations.

Variant displays