Original source

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

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

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

Most severe consequence
 
Upstream gene variant
Evidence status

Synonyms

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 8 transcripts and has 2602 sample genotypes.

Variant displays