rs587781756

Orientation

minus

Stabilized

minus

Geno	Mag	Summary
(C;C)	0	common in clinvar

Make rs587781756(C;T)

Make rs587781756(T;T)

Reference

GRCh38.p2 38.2/144

Chromosome

17

Position

35107017

Gene	RAD51D, RAD51L3-RFFL

is a	snp
is	mentioned by
dbSNP	rs587781756
dbSNP (classic)	rs587781756
ClinGen	rs587781756
ebi	rs587781756
HLI	rs587781756
Exac	rs587781756
Gnomad	rs587781756
Varsome	rs587781756
LitVar	rs587781756
Map	rs587781756
PheGenI	rs587781756
Biobank	rs587781756
1000 genomes	rs587781756
hgdp	rs587781756
ensembl	rs587781756
geneview	rs587781756
scholar	rs587781756
google	rs587781756
pharmgkb	rs587781756
gwascentral	rs587781756
openSNP	rs587781756
23andMe	rs587781756
SNPshot	rs587781756
SNPdbe	rs587781756
MSV3d	rs587781756
GWAS Ctlg	rs587781756

Max Magnitude

0

ClinVar
Risk	rs587781756(T;T)
Alt	rs587781756(T;T)
Reference	Rs587781756(C;C)
Significance	Pathogenic
Disease	Hereditary cancer-predisposing syndrome Breast-ovarian cancer not provided
Variation	info
Gene	RAD51D RAD51L3-RFFL
CLNDBN	Hereditary cancer-predisposing syndrome Breast-ovarian cancer, familial 4 not provided
Reversed	1
HGVS	NC_000017.10:g.33434036G>A
CLNSRC
CLNACC	RCV000129970.3, RCV000409676.1, RCV000485836.1,