Original source

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

Alleles
A/G | Ancestral: A | Ambiguity code: R | MAF: < 0.01 (G)
Location

Chromosome 20:6766782 (forward strand) | View in location tab

Most severe consequence
Evidence status

HGVS name

20:g.6766782A>G

About this variant

This variant overlaps 1 transcript and has 2504 individual genotypes.

Variation displays