Original source

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

C/A/G|Ancestral: G|Ambiguity code: V|MAF: 0.02 (A)

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

Most severe consequence
Intron variant
Evidence status


Archive dbSNP rs59360817

HGVS names

This variant has 40 HGVS names - Show

About this variant

This variant overlaps 50 transcripts and has 2781 sample genotypes.

Variant displays