Original source

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

G/A/T|Ancestral: G|Ambiguity code: D

Chromosome 11:6394204 (forward strand)|View in location tab

Co-located variants

HGMD-PUBLIC CM041858, CM910355

Most severe consequence
Missense variant
Evidence status

Clinical significance


This variant has 2 synonyms - Show

HGVS names

This variant has 22 HGVS names - Show

About this variant

This variant overlaps 54 transcripts and is associated with 5 phenotypes.

Variant displays