Original source

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

C/G | Ancestral: C | Ambiguity code: S

Chromosome 3:122433716 (forward strand) | View in location tab

Most severe consequence
Missense variant
Evidence status


Archive dbSNP rs11558302

HGVS names

This variant has 8 HGVS names - Show

About this variant

This variant overlaps 7 transcripts and has 263 sample genotypes.

Variant displays