Original source

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

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

Chromosome 13:23324513 (forward strand)|View in location tab

Co-located variants

HGMD-PUBLIC CM961273 ; PhenCode SGCG:c.848G>A (G/A)

Most severe consequence
Missense variant
Evidence status

Clinical significance


LSDB 16013, 2010_April_001_063_SGCG_608896_0002

HGVS names

This variant has 6 HGVS names - Show

About this variant

This variant overlaps 7 transcripts, 1 regulatory feature and is associated with 2 phenotypes.

Variant displays