rs759292615

Orientation

plus

Stabilized

plus

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

Make rs759292615(A;A)

Make rs759292615(A;C)

Reference

GRCh38.p2 38.2/147

Chromosome

17

Position

58732523

Gene	LOC105371843, RAD51C

is a	snp
is	mentioned by
dbSNP	rs759292615
dbSNP (classic)	rs759292615
ClinGen	rs759292615
ebi	rs759292615
HLI	rs759292615
Exac	rs759292615
Gnomad	rs759292615
Varsome	rs759292615
LitVar	rs759292615
Map	rs759292615
PheGenI	rs759292615
Biobank	rs759292615
1000 genomes	rs759292615
hgdp	rs759292615
ensembl	rs759292615
geneview	rs759292615
scholar	rs759292615
google	rs759292615
pharmgkb	rs759292615
gwascentral	rs759292615
openSNP	rs759292615
23andMe	rs759292615
SNPshot	rs759292615
SNPdbe	rs759292615
MSV3d	rs759292615
GWAS Ctlg	rs759292615

Max Magnitude

0

ClinVar
Risk	rs759292615(A;A)
Alt	rs759292615(A;A)
Reference	Rs759292615(C;C)
Significance	Probable-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.56809884C>A
CLNSRC
CLNACC	RCV000220031.1, RCV000232127.1,