Original source

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

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

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


with 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