Original source

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

Alleles
A/G | Ancestral: A | Ambiguity code: R | MAF: 0.27 (G)
Location

Chromosome 18:63098335 (forward strand) | View in location tab

Most severe consequence
Evidence status

HGVS name

18:g.63098335A>G

About this variant

This variant has 2504 individual genotypes.

Variation displays