This variation 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: 0.01 (G)
Location

This variation maps to 2 genomic locations; None selected

Evidence status

Clinical significance

This variation has 3 synonyms - click the plus to show

HGVS name

None

This variation has assays on 6 chips - click the plus to show

About this variant

This variant overlaps 1 transcript, has 2560 individual genotypes, is associated with 3 phenotypes and is mentioned in 2 citations.

Variation displays