Original source

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

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

Chromosome 9:336714 (forward strand)|View in location tab

Co-located variants

HGMD-PUBLIC CM098842, CS099677

Most severe consequence
Missense variant
Evidence status

Clinical significance


LSDB 16994

HGVS names

This variant has 16 HGVS names - Show

About this variant

This variant overlaps 9 transcripts and is associated with 2 phenotypes.

Variant displays