Original source

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

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

Chromosome 4:73853851 (forward strand) | View in location tab

Most severe consequence
Missense variant
Evidence status


Archive dbSNP rs3180519, rs1050941

HGVS names

This variant has 3 HGVS names - Show

About this variant

This variant overlaps 2 transcripts and has 2 sample genotypes.

Variant displays