Original source

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

Alleles
A/G|Ancestral: A|Ambiguity code: R|MAF: < 0.01 (G)
Location

Chromosome 1:11022209 (forward strand)|View in location tab

Co-located variant

HGMD-PUBLIC CM091848

Most severe consequence
 
Missense variant
Evidence status

Clinical significance

Synonyms

This variant has 2 synonyms - Show

HGVS names

This variant has 40 HGVS names - Show

About this variant

This variant overlaps 35 transcripts, has 2504 sample genotypes and is associated with 1 phenotype.

Variant displays