Original source

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

C/A/G | Ancestral: G | Ambiguity code: V | MAF: 0.20 (C)

Chromosome 11:3799953 (forward strand) | View in location tab

Most severe consequence
Intron variant
Evidence status


Archive dbSNP rs59360817

This variant has 40 HGVS names - click the plus to show

About this variant

This variant overlaps 50 transcripts and has 2549 sample genotypes.

Variant displays