Original source

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

Alleles
A/G|Ancestral: A|Ambiguity code: R|MAF: 0.38 (A)
Location

Chromosome 1:169476945 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs60163996, rs17577917

HGVS names

This variant has 3 HGVS names - Show

Genotyping chips

This variant has assays on 12 chips - Show

About this variant

This variant overlaps 3 transcripts, has 4297 sample genotypes and is associated with 1 phenotype.

Variant displays