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rs200293302

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs200293302(C;T)
Make rs200293302(T;T)
ReferenceGRCh38 38.1/142
Chromosome17
Position58703201
GeneRAD51C
is asnp
is mentioned by
dbSNPrs200293302
ebirs200293302
HLIrs200293302
Exacrs200293302
Varsomers200293302
Maprs200293302
PheGenIrs200293302
hapmaprs200293302
1000 genomesrs200293302
hgdprs200293302
ensemblrs200293302
gopubmedrs200293302
geneviewrs200293302
scholarrs200293302
googlers200293302
pharmgkbrs200293302
gwascentralrs200293302
openSNPrs200293302
23andMers200293302
23andMe allrs200293302
SNP Nexus

SNPshotrs200293302
SNPdbers200293302
MSV3drs200293302
GWAS Ctlgrs200293302
Max Magnitude0
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 RCV000129056.5, RCV000203684.1, RCV000212943.1,