Original source

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

A/T|Ancestral: A|Ambiguity code: W

Chromosome 14:73173587 (forward strand)|View in location tab

Co-located variants

HGMD-PUBLIC CM981652, CM961199

Most severe consequence
Missense variant
Evidence status

Clinical significance


PhenCode ADM_99, ADM_10

HGVS names

This variant has 24 HGVS names - Show

About this variant

This variant overlaps 22 transcripts and is associated with 3 phenotypes.

Variant displays