rs779582317

Orientation

plus

Stabilized

plus

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

Make rs779582317(A;C)

Make rs779582317(C;C)

Reference

GRCh38.p2 38.2/146

Chromosome

17

Position

58724038

Gene	LOC105371843, RAD51C

is a	snp
is	mentioned by
dbSNP	rs779582317
dbSNP (classic)	rs779582317
ClinGen	rs779582317
ebi	rs779582317
HLI	rs779582317
Exac	rs779582317
Gnomad	rs779582317
Varsome	rs779582317
LitVar	rs779582317
Map	rs779582317
PheGenI	rs779582317
Biobank	rs779582317
1000 genomes	rs779582317
hgdp	rs779582317
ensembl	rs779582317
geneview	rs779582317
scholar	rs779582317
google	rs779582317
pharmgkb	rs779582317
gwascentral	rs779582317
openSNP	rs779582317
23andMe	rs779582317
SNPshot	rs779582317
SNPdbe	rs779582317
MSV3d	rs779582317
GWAS Ctlg	rs779582317

Max Magnitude

0

ClinVar
Risk	rs779582317(C;C) rs779582317(G;G)
Alt	rs779582317(C;C) rs779582317(G;G)
Reference	Rs779582317(A;A)
Significance	Pathogenic
Disease	Fanconi anemia not provided
Variation	info
Gene	RAD51C
CLNDBN	Fanconi anemia, complementation group O not provided
Reversed	0
HGVS	NC_000017.10:g.56801399A>C; NC_000017.10:g.56801399A>G
CLNSRC
CLNACC	RCV000199789.1, RCV000236382.1, RCV000473356.1,