Original source

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

Alleles
C/T | Ancestral: T | Ambiguity code: Y | MAF: 0.39 (C)
Location

Chromosome 15:46593911 (forward strand) | View in location tab

Most severe consequence
 
Intergenic variant
Evidence status

Synonyms

Archive dbSNP rs61705220, rs1711619

HGVS name

15:g.46593911C>T

Genotyping chips

This variant has assays on: Affy GenomeWideSNP_6.0

About this variant

This variant has 3693 sample genotypes.

Variant displays