rs587782036

Orientation

plus

Stabilized

plus

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

Make rs587782036(C;C)

Make rs587782036(C;G)

Reference

GRCh38.p2 38.2/144

Chromosome

17

Position

58696692

Gene

RAD51C

is a	snp
is	mentioned by
dbSNP	rs587782036
dbSNP (classic)	rs587782036
ClinGen	rs587782036
ebi	rs587782036
HLI	rs587782036
Exac	rs587782036
Gnomad	rs587782036
Varsome	rs587782036
LitVar	rs587782036
Map	rs587782036
PheGenI	rs587782036
Biobank	rs587782036
1000 genomes	rs587782036
hgdp	rs587782036
ensembl	rs587782036
geneview	rs587782036
scholar	rs587782036
google	rs587782036
pharmgkb	rs587782036
gwascentral	rs587782036
openSNP	rs587782036
23andMe	rs587782036
SNPshot	rs587782036
SNPdbe	rs587782036
MSV3d	rs587782036
GWAS Ctlg	rs587782036

Max Magnitude

0

ClinVar
Risk	rs587782036(A;A) rs587782036(C;C)
Alt	rs587782036(A;A) rs587782036(C;C)
Reference	Rs587782036(G;G)
Significance	Probable-Pathogenic
Disease	Fanconi anemia Hereditary cancer-predisposing syndrome
Variation	info
Gene	RAD51C
CLNDBN	Fanconi anemia, complementation group O Hereditary cancer-predisposing syndrome
Reversed	0
HGVS	NC_000017.10:g.56774053G>A; NC_000017.10:g.56774053G>C
CLNSRC
CLNACC	RCV000477455.1, RCV000130492.3, RCV000204135.2,