Original source

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

Alleles
G/T | Ancestral: G | Ambiguity code: K | MAF: 0.03 (T)
Location

Chromosome 20:9067825 (forward strand) | View in location tab

Most severe consequence
Evidence status

HGVS name

20:g.9067825G>T

About this variant

This variant overlaps 5 transcripts and has 2504 individual genotypes.

Variation displays