Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | View in dbSNP

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

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

Most severe consequence
 
Missense variant
Evidence status

Synonyms

Archive dbSNP rs3180519, rs1050941

This variant has 3 HGVS names - click the plus to show

About this variant

This variant overlaps 2 transcripts and has 2 sample genotypes.

Variant displays