Original source

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

Alleles
C/T | Ancestral: C | Ambiguity code: Y | MAF: 0.29 (C)
Location

Chromosome 12:52313829 (forward strand) | View in location tab

Most severe consequence
Evidence status

HGVS name

12:g.52313829C>T

About this variant

This variant overlaps 3 transcripts and has 2514 individual genotypes.

Variation displays