rs876659394

Orientation

minus

Stabilized

minus

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

Make rs876659394(C;C)

Reference

GRCh38.p2 38.2/147

Chromosome

17

Position

35107364

Gene	RAD51D, RAD51L3-RFFL

is a	snp
is	mentioned by
dbSNP	rs876659394
dbSNP (classic)	rs876659394
ClinGen	rs876659394
ebi	rs876659394
HLI	rs876659394
Exac	rs876659394
Gnomad	rs876659394
Varsome	rs876659394
LitVar	rs876659394
Map	rs876659394
PheGenI	rs876659394
Biobank	rs876659394
1000 genomes	rs876659394
hgdp	rs876659394
ensembl	rs876659394
geneview	rs876659394
scholar	rs876659394
google	rs876659394
pharmgkb	rs876659394
gwascentral	rs876659394
openSNP	rs876659394
23andMe	rs876659394
SNPshot	rs876659394
SNPdbe	rs876659394
MSV3d	rs876659394
GWAS Ctlg	rs876659394

Max Magnitude

6

ClinVar
Risk	rs876659394(C;C)
Alt	rs876659394(C;C)
Reference	Rs876659394(T;T)
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.33434383A>G
CLNSRC
CLNACC	RCV000214604.1, RCV000233270.2,