Original source

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

Alleles
T/C | Ancestral: T | Ambiguity code: Y | MAF: 0.21 (C)
Location

Chromosome 17:13996570 (forward strand) | View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

This variant has 2 HGVS names - click the plus to show

17:g.13996570T>C
ENST00000602743.1:n.224+72702A>G

Genotyping chips

This variant has assays on: Affy GenomeWideSNP_6.0, Affy GeneChip 500K

About this variant

This variant overlaps 1 transcript and has 4310 sample genotypes.

Variant displays