Original source

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

Alleles
C/A/T | Ancestral: C | Ambiguity code: H
Location

Chromosome 1:26795056 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM106179, CM106178

Most severe consequence
Evidence status

Clinical significance

This variation has 12 HGVS names - click the plus to show

About this variant

This variant overlaps 12 transcripts and is associated with 4 phenotypes.

Variation displays