rs587782533

Orientation

plus

Stabilized

plus

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

Make rs587782533(-;-)

Make rs587782533(-;C)

Reference

GRCh38.p2 38.2/144

Chromosome

17

Position

58694943

Gene

RAD51C

is a	snp
is	mentioned by
dbSNP	rs587782533
dbSNP (classic)	rs587782533
ClinGen	rs587782533
ebi	rs587782533
HLI	rs587782533
Exac	rs587782533
Gnomad	rs587782533
Varsome	rs587782533
LitVar	rs587782533
Map	rs587782533
PheGenI	rs587782533
Biobank	rs587782533
1000 genomes	rs587782533
hgdp	rs587782533
ensembl	rs587782533
geneview	rs587782533
scholar	rs587782533
google	rs587782533
pharmgkb	rs587782533
gwascentral	rs587782533
openSNP	rs587782533
23andMe	rs587782533
SNPshot	rs587782533
SNPdbe	rs587782533
MSV3d	rs587782533
GWAS Ctlg	rs587782533

Max Magnitude

0

ClinVar
Risk	rs587782533(-;-)
Alt	rs587782533(-;-)
Reference	Rs587782533(C;C)
Significance	Pathogenic
Disease	Hereditary cancer-predisposing syndrome
Variation	info
Gene	RAD51C
CLNDBN	Hereditary cancer-predisposing syndrome
Reversed	0
HGVS	NC_000017.10:g.56772304delC
CLNSRC
CLNACC	RCV000131735.2,