Original source

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

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

Chromosome 15:63060899 (forward strand)|View in location tab

Co-located variants

HGMD-PUBLIC CM941333 ; PhenCode FHC0622 (G/A)

Most severe consequence
Missense variant
Evidence status

Clinical significance


This variant has 6 synonyms - Show

HGVS names

This variant has 43 HGVS names - Show

About this variant

This variant overlaps 32 transcripts, is associated with 5 phenotypes and is mentioned in 19 citations.

Variant displays