Original source

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

Alleles
G/A/T|Ancestral: G|Ambiguity code: D|MAF: 0.44 (T)
Location

Chromosome 1:155290592 (forward strand)|View in location tab

Most severe consequence
 
Missense variant
Evidence status

Synonyms
HGVS names

This variant has 10 HGVS names - Show

Genotyping chips

This variant has assays on 10 chips - Show

About this variant

This variant overlaps 14 transcripts, has 4450 sample genotypes, is associated with 1 phenotype and is mentioned in 2 citations.

Variant displays