Original source

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

Alleles
A/C/G|Ancestral: A|Ambiguity code: V|MAF: 0.44 (G)
Location

Chromosome 1:155290559 (forward strand)|View in location tab

Most severe consequence
 
3 prime UTR variant
Evidence status

Synonyms

Archive dbSNP rs60725763, rs3192608

HGVS names

This variant has 6 HGVS names - Show

Genotyping chips

This variant has assays on 6 chips - Show

About this variant

This variant overlaps 14 transcripts, has 3780 sample genotypes, is associated with 1 phenotype and is mentioned in 4 citations.

Variant displays