rs786203137

Orientation

minus

Stabilized

minus

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

Make rs786203137(-;-)

Make rs786203137(-;GT)

Reference

GRCh38.p2 38.2/146

Chromosome

17

Position

35119160

Gene	RAD51D, RAD51L3-RFFL

is a	snp
is	mentioned by
dbSNP	rs786203137
dbSNP (classic)	rs786203137
ClinGen	rs786203137
ebi	rs786203137
HLI	rs786203137
Exac	rs786203137
Gnomad	rs786203137
Varsome	rs786203137
LitVar	rs786203137
Map	rs786203137
PheGenI	rs786203137
Biobank	rs786203137
1000 genomes	rs786203137
hgdp	rs786203137
ensembl	rs786203137
geneview	rs786203137
scholar	rs786203137
google	rs786203137
pharmgkb	rs786203137
gwascentral	rs786203137
openSNP	rs786203137
23andMe	rs786203137
SNPshot	rs786203137
SNPdbe	rs786203137
MSV3d	rs786203137
GWAS Ctlg	rs786203137

Max Magnitude

0

ClinVar
Risk	rs786203137(-;-)
Alt	rs786203137(-;-)
Reference	Rs786203137(GT;GT)
Significance	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.33446179_33446180delAC
CLNSRC
CLNACC	RCV000166313.2, RCV000469049.1,