Original source

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

Alleles
T/C|Ancestral: C|Ambiguity code: Y|MAF: 0.10 (C)
Location

Chromosome 17:34355597 (forward strand)|View in location tab

Co-located variant

HGMD-PUBLIC CR035881

Most severe consequence
 
Upstream gene variant
Evidence status

HGVS name

17:g.34355597T>C

Genotyping chips

This variant has assays on 6 chips - Show

About this variant

This variant overlaps 3 transcripts and has 3690 sample genotypes.

Variant displays