Original source

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

Alleles
G/C|Ambiguity code: S
Location

Chromosome 3:10334574 (forward strand)|View in location tab

Most severe consequence
 
Missense variant
Evidence status

HGVS names

This variant has 4 HGVS names - Show

About this variant

This variant overlaps 6 transcripts and has 42 sample genotypes.

Variant displays