Original source

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

Alleles
A/C | Ancestral: A | Ambiguity code: M | MAF: 0.03 (C)
Location

Chromosome 12:52674687 (forward strand) | View in location tab

Most severe consequence
 
Downstream gene variant
Evidence status

Synonyms

Archive dbSNP rs386604842

HGVS name

12:g.52674687A>C

This variant has assays on 4 chips - click the plus to show

About this variant

This variant overlaps 2 transcripts and has 3534 sample genotypes.

Variant displays