Original source

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

Alleles
G/T|Ancestral: G|Ambiguity code: K|MAF: 0.33 (T)
Location

Chromosome 1:7982766 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms
HGVS names

This variant has 8 HGVS names - Show

Genotyping chips

This variant has assays on 6 chips - Show

About this variant

This variant overlaps 8 transcripts, 2 regulatory features, has 3760 sample genotypes, is associated with 1 phenotype and is mentioned in 2 citations.

Variant displays