rs587782702

Orientation

plus

Stabilized

plus

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

Make rs587782702(G;T)

Make rs587782702(T;T)

Reference

GRCh38.p2 38.2/144

Chromosome

17

Position

58720817

Gene

RAD51C

is a	snp
is	mentioned by
dbSNP	rs587782702
dbSNP (classic)	rs587782702
ClinGen	rs587782702
ebi	rs587782702
HLI	rs587782702
Exac	rs587782702
Gnomad	rs587782702
Varsome	rs587782702
LitVar	rs587782702
Map	rs587782702
PheGenI	rs587782702
Biobank	rs587782702
1000 genomes	rs587782702
hgdp	rs587782702
ensembl	rs587782702
geneview	rs587782702
scholar	rs587782702
google	rs587782702
pharmgkb	rs587782702
gwascentral	rs587782702
openSNP	rs587782702
23andMe	rs587782702
SNPshot	rs587782702
SNPdbe	rs587782702
MSV3d	rs587782702
GWAS Ctlg	rs587782702

Max Magnitude

0

ClinVar
Risk	rs587782702(T;T)
Alt	rs587782702(T;T)
Reference	Rs587782702(G;G)
Significance	Other
Disease	Breast-ovarian cancer Hereditary cancer-predisposing syndrome Fanconi anemia not provided
Variation	info
Gene	RAD51C
CLNDBN	Breast-ovarian cancer, familial 3 Hereditary cancer-predisposing syndrome Fanconi anemia, complementation group O not provided
Reversed	0
HGVS	NC_000017.10:g.56798178G>T
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000007225.2, RCV000132144.3, RCV000225845.2, RCV000484863.1,