Original source

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

Alleles
T/C | Ancestral: C | Ambiguity code: Y | MAF: 0.46 (C)
Location

Chromosome 12:51186436 (forward strand) | View in location tab

Most severe consequence
 
Downstream gene variant
Evidence status

Synonyms

Archive dbSNP rs58837806

HGVS name

12:g.51186436T>C

This variant has assays on 9 chips - click the plus to show

About this variant

This variant overlaps 3 transcripts and has 3690 sample genotypes.

Variant displays