Original source

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

C/G | Ancestral: C | Ambiguity code: S | MAF: 0.11 (G)

Chromosome 4:89772325 (forward strand) | View in location tab

Most severe consequence
Intron variant
Evidence status


Archive dbSNP rs17796079

HGVS names

This variant has 12 HGVS names - Show

About this variant

This variant overlaps 11 transcripts, has 3116 sample genotypes and is mentioned in 2 citations.

Variant displays