Original source

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

A/C | Ancestral: C | Ambiguity code: M | MAF: < 0.01 (A)

Chromosome 15:64163961 (forward strand) | View in location tab

Most severe consequence
Upstream gene variant
Evidence status


Archive dbSNP rs59155550

HGVS names

This variant has 2 HGVS names - Show

Genotyping chips

This variant has assays on 5 chips - Show

About this variant

This variant overlaps 6 transcripts and has 2602 sample genotypes.

Variant displays