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rs745797941

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs745797941(C;T)
Make rs745797941(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome5
Position132637179
GeneRAD50, TH2LCRR
is asnp
is mentioned by
dbSNPrs745797941
ClinGenrs745797941
ebirs745797941
HLIrs745797941
Exacrs745797941
Varsomers745797941
Maprs745797941
PheGenIrs745797941
hapmaprs745797941
1000 genomesrs745797941
hgdprs745797941
ensemblrs745797941
gopubmedrs745797941
geneviewrs745797941
scholarrs745797941
googlers745797941
pharmgkbrs745797941
gwascentralrs745797941
openSNPrs745797941
23andMers745797941
23andMe allrs745797941
SNP Nexus

SNPshotrs745797941
SNPdbers745797941
MSV3drs745797941
GWAS Ctlgrs745797941
Max Magnitude0
ClinVar
Risk rs745797941(T;T)
Alt rs745797941(T;T)
Reference Rs745797941(C;C)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene TH2LCRR RAD50
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000005.9:g.131972871C>T
CLNSRC
CLNACC RCV000222027.1,