Original source

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

A/G | Ambiguity code: R | MAF: 0.49 (G)

Chromosome 11:2312445 (forward strand) | View in location tab

Most severe consequence
Intron variant
Evidence status


Archive dbSNP rs59656042

HGVS names

This variant has 16 HGVS names - Show

Genotyping chips

This variant has assays on 6 chips - Show

About this variant

This variant overlaps 17 transcripts, 1 regulatory feature, has 3690 sample genotypes and is mentioned in 1 citation.

Variant displays