Original source

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

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

Chromosome 1:226885603 (forward strand)|View in location tab

Co-located variant

HGMD-PUBLIC CM951087

Most severe consequence
 
Missense variant
Evidence status

Clinical significance

Synonyms

This variant has 3 synonyms - Show

HGVS names

This variant has 11 HGVS names - Show

About this variant

This variant overlaps 9 transcripts, is associated with 3 phenotypes and is mentioned in 4 citations.

Variant displays