Original source

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

C/T | Ancestral: T | Ambiguity code: Y | MAF: 0.46 (T)

Chromosome 17:48729772 (forward strand) | View in location tab

Most severe consequence
Upstream gene variant
Evidence status

HGVS names

This variant has 2 HGVS names - Show

Genotyping chips

This variant has assays on: Affy GenomeWideSNP_6.0, Illumina_CytoSNP12v1

About this variant

This variant overlaps 3 transcripts, has 3807 sample genotypes and is mentioned in 1 citation.

Variant displays