Original source

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

Alleles
C/A|Ancestral: C|Ambiguity code: M|MAF: 0.28 (A)
Location

Chromosome 1:158421044 (forward strand)|View in location tab

Most severe consequence
 
Upstream gene variant
Evidence status

Synonyms

Archive dbSNP rs17627966, rs61168072

HGVS name

1:g.158421044C>A

Genotyping chips

This variant has assays on 9 chips - Show

About this variant

This variant overlaps 1 transcript and has 3733 sample genotypes.

Variant displays