Original source

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

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

Chromosome 10:72007506 (forward strand)|View in location tab

Co-located variant

HGMD-PUBLIC CM105996

Most severe consequence
 
Missense variant
Evidence status

Clinical significance

Synonyms

LSDB 21088

HGVS names

This variant has 3 HGVS names - Show

About this variant

This variant overlaps 1 transcript and is associated with 2 phenotypes.

Variant displays