Original source

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

C/T | Ancestral: T | Ambiguity code: Y | MAF: 0.34 (C)

Chromosome 22:29289722 (forward strand) | View in location tab

Most severe consequence
Non coding transcript exon variant
Evidence status


Archive dbSNP rs1008239, rs60985891, rs861938

HGVS names

This variant has 11 HGVS names - Show

About this variant

This variant overlaps 16 transcripts and has 2508 sample genotypes.

Variant displays