Original source

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

Alleles
T/G | Ancestral: T | Ambiguity code: K | MAF: < 0.01 (G)
Location

Chromosome 18:63098712 (forward strand) | View in location tab

Most severe consequence
 
Intergenic variant
Evidence status

HGVS name

18:g.63098712T>G

About this variant

This variant has 2504 sample genotypes.

Variant displays