Original source

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

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

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