Original source

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

Alleles
C/G/T|Ancestral: C|Ambiguity code: B
Location

Chromosome 15:38349482 (forward strand)|View in location tab

Co-located variant

HGMD-PUBLIC CM074581

Most severe consequence
 
Stop gained
Evidence status

Clinical significance

Synonyms

LSDB 16208

HGVS names

This variant has 6 HGVS names - Show

About this variant

This variant overlaps 2 transcripts, 1 regulatory feature and is associated with 2 phenotypes.

Variant displays