Original source

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

G/A | Ancestral: G | Ambiguity code: R | MAF: 0.41 (A)

Chromosome 11:46043423 (forward strand) | View in location tab

Most severe consequence
Intron variant
Evidence status


Archive dbSNP rs17530765

HGVS names

This variant has 8 HGVS names - Show

Genotyping chips

This variant has assays on: Illumina_Human1M-duo, Illumina_HumanOmni5

About this variant

This variant overlaps 7 transcripts and has 4022 sample genotypes.

Variant displays