Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | 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

This variant has 16 HGVS names - click the plus to show

This variant has assays on 6 chips - click the plus to show

About this variant

This variant overlaps 17 transcripts, 1 regulatory feature, has 2571 sample genotypes and is mentioned in 1 citation.

Variant displays