Original source

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

A/G | Ancestral: A | Ambiguity code: R | MAF: 0.45 (G)

Chromosome 11:116837304 (forward strand) | View in location tab

Most severe consequence
Intron variant
Evidence status


Archive dbSNP rs17249484, rs61758322

HGVS names

This variant has 9 HGVS names - Show

About this variant

This variant overlaps 10 transcripts, 1 regulatory feature, has 2533 sample genotypes and is mentioned in 5 citations.

Variant displays