Original source

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

Alleles
C/T | Ancestral: T | Ambiguity code: Y | MAF: 0.35 (T)
Location

Chromosome 10:31528977 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs52825274, rs18841, rs58911991

This variation has 6 HGVS names - click the plus to show

This variation has assays on 7 chips - click the plus to show

About this variant

This variant overlaps 11 transcripts, has 2792 individual genotypes and is mentioned in 5 citations.

Variation displays