Original source

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

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

Chromosome 10:100989154 (forward strand)|View in location tab

Co-located variants

HGMD-PUBLIC CM085294, CM012072

Most severe consequence
Stop gained
Evidence status

Clinical significance


LSDB 2010_April_001_065_PEO1_606075_0005, 13529

HGVS names

This variant has 16 HGVS names - Show

About this variant

This variant overlaps 54 transcripts and is associated with 2 phenotypes.

Variant displays