Original source

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

Alleles
T/G|Ancestral: T|Ambiguity code: K|MAF: 0.07 (G)
Location

Chromosome 11:101584417 (forward strand)|View in location tab

Co-located variant

HGMD-PUBLIC CR099422

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 6 transcripts and has 2507 sample genotypes.

Variant displays