rs587781287

Orientation

plus

Stabilized

plus

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

Make rs587781287(C;T)

Make rs587781287(T;T)

Reference

GRCh38.p2 38.2/144

Chromosome

17

Position

58724090

Gene	LOC105371843, RAD51C

is a	snp
is	mentioned by
dbSNP	rs587781287
dbSNP (classic)	rs587781287
ClinGen	rs587781287
ebi	rs587781287
HLI	rs587781287
Exac	rs587781287
Gnomad	rs587781287
Varsome	rs587781287
LitVar	rs587781287
Map	rs587781287
PheGenI	rs587781287
Biobank	rs587781287
1000 genomes	rs587781287
hgdp	rs587781287
ensembl	rs587781287
geneview	rs587781287
scholar	rs587781287
google	rs587781287
pharmgkb	rs587781287
gwascentral	rs587781287
openSNP	rs587781287
23andMe	rs587781287
SNPshot	rs587781287
SNPdbe	rs587781287
MSV3d	rs587781287
GWAS Ctlg	rs587781287

Max Magnitude

0

ClinVar
Risk	rs587781287(T;T)
Alt	rs587781287(T;T)
Reference	Rs587781287(C;C)
Significance	Pathogenic
Disease	Hereditary cancer-predisposing syndrome Fanconi anemia not provided
Variation	info
Gene	RAD51C
CLNDBN	Hereditary cancer-predisposing syndrome Fanconi anemia, complementation group O not provided
Reversed	0
HGVS	NC_000017.10:g.56801451C>T
CLNSRC
CLNACC	RCV000128973.4, RCV000230603.1, RCV000483841.1,