Original source

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

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

Chromosome 11:72243821 (forward strand)|View in location tab

Most severe consequence
 
Missense variant
HGVS names

This variant has 4 HGVS names - Show

About this variant

This variant overlaps 7 transcripts and 1 regulatory feature.

Variant displays