Original source

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

Alleles
T/-|Ancestral: T|MAF: 0.36 (T)
Location

Chromosome 18:903130 (forward strand)|View in location tab

Most severe consequence
 
Non coding transcript exon variant
Evidence status

HGVS names

This variant has 3 HGVS names - Show

About this variant

This variant overlaps 9 transcripts and has 2510 sample genotypes.

Variant displays