This variant maps to 2 locations

Select a location:
Original source

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

Alleles
T/G | Ancestral: T | Ambiguity code: K | MAF: 0.28 (G)
Location

This variant maps to 2 genomic locations; None selected

Evidence status

Clinical significance

This variant has 8 synonyms - click the plus to show

HGVS name

None

This variant has assays on 10 chips - click the plus to show

About this variant

This variant has 4036 sample genotypes, is associated with 8 phenotypes and is mentioned in 5 citations.

Variant displays