This variant maps to 7 locations

Select a location:
Original source

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

Alleles
C/T|Ancestral: C|Ambiguity code: Y|MAF: 0.10 (T)
Location

This variant maps to 7 genomic locations; None selected

Evidence status

HGVS name

None

Genotyping chips

This variant has assays on 5 chips - Show

About this variant

This variant overlaps 1 regulatory feature, has 3623 sample genotypes, is associated with 7 phenotypes and is mentioned in 125 citations.

Variant displays