rs786203945

Orientation

plus

Stabilized

plus

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

Make rs786203945(-;-)

Make rs786203945(-;CT)

Reference

GRCh38.p2 38.2/146

Chromosome

17

Position

58694966

Gene

RAD51C

is a	snp
is	mentioned by
dbSNP	rs786203945
dbSNP (classic)	rs786203945
ClinGen	rs786203945
ebi	rs786203945
HLI	rs786203945
Exac	rs786203945
Gnomad	rs786203945
Varsome	rs786203945
LitVar	rs786203945
Map	rs786203945
PheGenI	rs786203945
Biobank	rs786203945
1000 genomes	rs786203945
hgdp	rs786203945
ensembl	rs786203945
geneview	rs786203945
scholar	rs786203945
google	rs786203945
pharmgkb	rs786203945
gwascentral	rs786203945
openSNP	rs786203945
23andMe	rs786203945
SNPshot	rs786203945
SNPdbe	rs786203945
MSV3d	rs786203945
GWAS Ctlg	rs786203945

Merged from

Rs754525165

Max Magnitude

0

ClinVar
Risk	rs786203945(-;-)
Alt	rs786203945(-;-)
Reference	Rs786203945(CT;CT)
Significance	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.56772327_56772328delCT
CLNSRC
CLNACC	RCV000167466.1, RCV000456496.1,