rs786202251

Orientation

minus

Stabilized

minus

Geno	Mag	Summary
(-;C)	6	Ovarian cancer susceptibility
(C;C)	0	common in clinvar

Make rs786202251(-;-)

Reference

GRCh38.p2 38.2/146

Chromosome

17

Position

35101206

Gene	RAD51D, RAD51L3-RFFL

is a	snp
is	mentioned by
dbSNP	rs786202251
dbSNP (classic)	rs786202251
ClinGen	rs786202251
ebi	rs786202251
HLI	rs786202251
Exac	rs786202251
Gnomad	rs786202251
Varsome	rs786202251
LitVar	rs786202251
Map	rs786202251
PheGenI	rs786202251
Biobank	rs786202251
1000 genomes	rs786202251
hgdp	rs786202251
ensembl	rs786202251
geneview	rs786202251
scholar	rs786202251
google	rs786202251
pharmgkb	rs786202251
gwascentral	rs786202251
openSNP	rs786202251
23andMe	rs786202251
SNPshot	rs786202251
SNPdbe	rs786202251
MSV3d	rs786202251
GWAS Ctlg	rs786202251

Max Magnitude

6

ClinVar
Risk	rs786202251(-;-)
Alt	rs786202251(-;-)
Reference	Rs786202251(C;C)
Significance	Probable-Pathogenic
Disease	Hereditary cancer-predisposing syndrome Breast-ovarian cancer
Variation	info
Gene	RAD51D RAD51L3-RFFL
CLNDBN	Hereditary cancer-predisposing syndrome Breast-ovarian cancer, familial 4
Reversed	1
HGVS	NC_000017.10:g.33428225delG
CLNSRC
CLNACC	RCV000164969.1, RCV000467554.1,