Original source

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

Alleles
G/T | Ancestral: G | Ambiguity code: K | MAF: 0.06 (T)
Location

Chromosome 12:20808727 (forward strand) | View in location tab

Most severe consequence
Evidence status

HGVS name

12:g.20808727G>T

About this variant

This variant overlaps 2 transcripts and has 2505 individual genotypes.

Variation displays