Original source

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

G/A | Ancestral: G | Ambiguity code: R

Chromosome 11:116837018 (forward strand) | View in location tab

Most severe consequence
Synonymous variant
Evidence status


Archive dbSNP rs9692, rs3209633, rs11542978

HGVS names

This variant has 14 HGVS names - Show

About this variant

This variant overlaps 10 transcripts and 1 regulatory feature.

Variant displays