rs587781410

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(AGT;AGT)	0	common in clinvar
(GTA;GTA)	0	common in clinvar
(I;I)	0	common genotype

Make rs587781410(-;-)

Make rs587781410(-;GTA)

Reference

GRCh38.p2 38.2/147

Chromosome

17

Position

58732549

Gene	LOC105371843, RAD51C

is a	snp
is	mentioned by
dbSNP	rs587781410
dbSNP (classic)	rs587781410
ClinGen	rs587781410
ebi	rs587781410
HLI	rs587781410
Exac	rs587781410
Gnomad	rs587781410
Varsome	rs587781410
LitVar	rs587781410
Map	rs587781410
PheGenI	rs587781410
Biobank	rs587781410
1000 genomes	rs587781410
hgdp	rs587781410
ensembl	rs587781410
geneview	rs587781410
scholar	rs587781410
google	rs587781410
pharmgkb	rs587781410
gwascentral	rs587781410
openSNP	rs587781410
23andMe	rs587781410
SNPshot	rs587781410
SNPdbe	rs587781410
MSV3d	rs587781410
GWAS Ctlg	rs587781410

Max Magnitude

0

Mentioned as a pathogenic/likely pathogenic mutation associated with cancer predisposition in [PMID 26681312]

ClinVar
Risk	rs587781410(-;-) Rs587781410(AGT;AGT)
Alt	rs587781410(-;-) Rs587781410(AGT;AGT)
Reference	Rs587781410(GTA;GTA)
Significance	Pathogenic
Disease	Hereditary cancer-predisposing syndrome Fanconi anemia not provided Breast-ovarian cancer
Variation	info
Gene	RAD51C
CLNDBN	Hereditary cancer-predisposing syndrome Fanconi anemia, complementation group O not provided Breast-ovarian cancer, familial 3
Reversed	0
HGVS	NC_000017.10:g.56809910_56809912delGTA
CLNSRC
CLNACC	RCV000116170.7, RCV000197293.4, RCV000235204.2, RCV000456115.1,