Original source

Variants (including SNPs and indels) imported from dbSNP (mapped to GRCh38) (release 138) | View in dbSNP

Alleles
T/C | Ancestral: C | Ambiguity code: Y | MAF: 0.09 (C)
Location

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

Co-located

with HGMD-PUBLIC CR035881

Most severe consequence
Evidence status

HGVS name

17:g.34355597T>C

This variation has assays on 5 chips - click the plus to show

Variation displays