rs200293302

Orientation

plus

Stabilized

plus

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

Make rs200293302(C;T)

Make rs200293302(T;T)

Reference

GRCh38 38.1/142

Chromosome

17

Position

58703201

Gene

RAD51C

is a	snp
is	mentioned by
dbSNP	rs200293302
dbSNP (classic)	rs200293302
ClinGen	rs200293302
ebi	rs200293302
HLI	rs200293302
Exac	rs200293302
Gnomad	rs200293302
Varsome	rs200293302
LitVar	rs200293302
Map	rs200293302
PheGenI	rs200293302
Biobank	rs200293302
1000 genomes	rs200293302
hgdp	rs200293302
ensembl	rs200293302
geneview	rs200293302
scholar	rs200293302
google	rs200293302
pharmgkb	rs200293302
gwascentral	rs200293302
openSNP	rs200293302
23andMe	rs200293302
SNPshot	rs200293302
SNPdbe	rs200293302
MSV3d	rs200293302
GWAS Ctlg	rs200293302

Max Magnitude

0

ClinVar
Risk	rs200293302(T;T)
Alt	rs200293302(T;T)
Reference	Rs200293302(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.56780562C>T
CLNSRC	Inc.
CLNACC	RCV000129056.6, RCV000203684.3, RCV000212943.3,