Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | 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

This variant has assays on 11 chips - click the plus to show

About this variant

This variant overlaps 2 transcripts and has 4035 sample genotypes.

Variant displays