rs587782736

Orientation

minus

Stabilized

minus

Geno	Mag	Summary
(-;-)	0	common in clinvar
(-;AA)	6	Ovarian cancer susceptibility
(D;D)	0	common genotype

Make rs587782736(AA;AA)

Reference

GRCh38.p2 38.2/144

Chromosome

17

Position

35119114

Gene	RAD51D, RAD51L3-RFFL

is a	snp
is	mentioned by
dbSNP	rs587782736
dbSNP (classic)	rs587782736
ClinGen	rs587782736
ebi	rs587782736
HLI	rs587782736
Exac	rs587782736
Gnomad	rs587782736
Varsome	rs587782736
LitVar	rs587782736
Map	rs587782736
PheGenI	rs587782736
Biobank	rs587782736
1000 genomes	rs587782736
hgdp	rs587782736
ensembl	rs587782736
geneview	rs587782736
scholar	rs587782736
google	rs587782736
pharmgkb	rs587782736
gwascentral	rs587782736
openSNP	rs587782736
23andMe	rs587782736
SNPshot	rs587782736
SNPdbe	rs587782736
MSV3d	rs587782736
GWAS Ctlg	rs587782736

Max Magnitude

6

ClinVar
Risk	rs587782736(AA;AA)
Alt	rs587782736(AA;AA)
Reference	Rs587782736(-;-)
Significance	Pathogenic
Disease	Hereditary cancer-predisposing syndrome
Variation	info
Gene	RAD51D RAD51L3-RFFL
CLNDBN	Hereditary cancer-predisposing syndrome
Reversed	1
HGVS	NC_000017.10:g.33446133_33446134insTT
CLNSRC
CLNACC	RCV000132237.3,