Original source

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

Alleles
A/C|Ancestral: C|Ambiguity code: M|MAF: 0.34 (A)
Location

Chromosome 1:150646156 (forward strand)|View in location tab

Most severe consequence
 
Downstream gene variant
Evidence status

Synonyms

Archive dbSNP rs60505777

HGVS name

1:g.150646156A>C

Genotyping chips

This variant has assays on 11 chips - Show

About this variant

This variant overlaps 2 transcripts and has 4035 sample genotypes.

Variant displays