rs587780259

Orientation

plus

Stabilized

plus

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

Make rs587780259(A;G)

Make rs587780259(G;G)

Reference

GRCh38.p2 38.2/144

Chromosome

17

Position

58709857

Gene

RAD51C

is a	snp
is	mentioned by
dbSNP	rs587780259
dbSNP (classic)	rs587780259
ClinGen	rs587780259
ebi	rs587780259
HLI	rs587780259
Exac	rs587780259
Gnomad	rs587780259
Varsome	rs587780259
LitVar	rs587780259
Map	rs587780259
PheGenI	rs587780259
Biobank	rs587780259
1000 genomes	rs587780259
hgdp	rs587780259
ensembl	rs587780259
geneview	rs587780259
scholar	rs587780259
google	rs587780259
pharmgkb	rs587780259
gwascentral	rs587780259
openSNP	rs587780259
23andMe	rs587780259
SNPshot	rs587780259
SNPdbe	rs587780259
MSV3d	rs587780259
GWAS Ctlg	rs587780259

Max Magnitude

0

ClinVar
Risk	rs587780259(G;G)
Alt	rs587780259(G;G)
Reference	Rs587780259(A;A)
Significance	Other
Disease	Hereditary cancer-predisposing syndrome Fanconi anemia not provided Breast-ovarian cancer
Variation	info
Gene	RAD51C
CLNDBN	Hereditary cancer-predisposing syndrome Fanconi anemia, complementation group O not provided Breast-ovarian cancer, familial 3
Reversed	0
HGVS	NC_000017.10:g.56787218A>G
CLNSRC
CLNACC	RCV000116178.5, RCV000234445.2, RCV000254687.2, RCV000456123.1,