Original source

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

T/C | Ancestral: T | Ambiguity code: Y | MAF: 0.11 (C)

Chromosome 22:31947860 (forward strand) | View in location tab

Most severe consequence
Intron variant
Evidence status


Archive dbSNP rs17676137

HGVS names

This variant has 7 HGVS names - Show

About this variant

This variant overlaps 8 transcripts, has 3141 sample genotypes and is mentioned in 1 citation.

Variant displays