rs587782818

Orientation

plus

Stabilized

plus

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

Make rs587782818(C;G)

Make rs587782818(G;G)

Reference

GRCh38.p2 38.2/144

Chromosome

17

Position

58703325

Gene

RAD51C

is a	snp
is	mentioned by
dbSNP	rs587782818
dbSNP (classic)	rs587782818
ClinGen	rs587782818
ebi	rs587782818
HLI	rs587782818
Exac	rs587782818
Gnomad	rs587782818
Varsome	rs587782818
LitVar	rs587782818
Map	rs587782818
PheGenI	rs587782818
Biobank	rs587782818
1000 genomes	rs587782818
hgdp	rs587782818
ensembl	rs587782818
geneview	rs587782818
scholar	rs587782818
google	rs587782818
pharmgkb	rs587782818
gwascentral	rs587782818
openSNP	rs587782818
23andMe	rs587782818
SNPshot	rs587782818
SNPdbe	rs587782818
MSV3d	rs587782818
GWAS Ctlg	rs587782818

Max Magnitude

0

ClinVar
Risk	rs587782818(G;G)
Alt	rs587782818(G;G)
Reference	Rs587782818(C;C)
Significance	Pathogenic
Disease	Hereditary cancer-predisposing syndrome Fanconi anemia
Variation	info
Gene	RAD51C
CLNDBN	Hereditary cancer-predisposing syndrome Fanconi anemia, complementation group O
Reversed	0
HGVS	NC_000017.10:g.56780686C>G
CLNSRC
CLNACC	RCV000132392.3, RCV000458376.1,