Original source

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

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

Chromosome 14:23429005 (forward strand)|View in location tab

Co-located variants

COSMIC COSM2031862 ; HGMD-PUBLIC CM920490, CM087715 ; PhenCode FHC0121 (G/A)

Most severe consequence
Missense variant
Evidence status

Clinical significance


LSDB 29168, 4195

HGVS names

This variant has 12 HGVS names - Show

About this variant

This variant overlaps 4 transcripts and is associated with 7 phenotypes.

Variant displays