This variant maps to 3 locations

Select a location:
Original source

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

Alleles
A/T | Ancestral: T | Ambiguity code: W | MAF: 0.09 (T)
Location

This variant maps to 3 genomic locations; None selected

Evidence status

Synonyms

Archive dbSNP rs118164267

HGVS name

None

About this variant

This variant overlaps 1 regulatory feature, has 2801 sample genotypes and is mentioned in 1 citation.

Variant displays