Original source

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

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

Chromosome 10:100989352 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM012079

Most severe consequence
 
Missense variant
Evidence status

Clinical significance

Synonyms

LSDB 13531, 2010_April_001_067_PEO1_606075_0007

This variant has 16 HGVS names - click the plus to show

About this variant

This variant overlaps 54 transcripts and is associated with 2 phenotypes.

Variant displays