Original source

Variants (including SNPs and indels) imported from dbSNP (release 144)|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
 
Intergenic variant
Evidence status

HGVS name

18:g.63098335A>G

About this variant

This variant has 2504 sample genotypes.

Variant displays