Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | View in dbSNP

Alleles
C/T | Ancestral: C | Ambiguity code: Y
Location

Chromosome 10:23193805 (forward strand) | View in location tab

Co-located

with COSMIC COSM917084 (C/T) ; HGMD-PUBLIC CM043069

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 14692, 2010_April_001_090_PTF1A_607194_0001

This variation has 3 HGVS names - click the plus to show

About this variant

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

Variation displays