Original source

Variants (including SNPs and indels) imported from dbSNP (release 144)|View in dbSNP

Alleles
T/C|Ancestral: T|Ambiguity code: Y|MAF: < 0.01 (C)
Location

Chromosome 18:63098448 (forward strand)|View in location tab

Most severe consequence
 
Intergenic variant
Evidence status

HGVS name

18:g.63098448T>C

About this variant

This variant has 2504 sample genotypes.

Variant displays