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rs149201802

From SNPedia

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Geno Mag Summary
(C;C) 0 common in clinvar
Make rs149201802(C;T)
Make rs149201802(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome5
Position132594950
GeneRAD50
is asnp
is mentioned by
dbSNPrs149201802
ebirs149201802
HLIrs149201802
Exacrs149201802
Varsomers149201802
Maprs149201802
PheGenIrs149201802
hapmaprs149201802
1000 genomesrs149201802
hgdprs149201802
ensemblrs149201802
gopubmedrs149201802
geneviewrs149201802
scholarrs149201802
googlers149201802
pharmgkbrs149201802
gwascentralrs149201802
openSNPrs149201802
23andMers149201802
23andMe allrs149201802
SNP Nexus

SNPshotrs149201802
SNPdbers149201802
MSV3drs149201802
GWAS Ctlgrs149201802
Max Magnitude0
ClinVar
Risk rs149201802(G,T;G,T)
Alt rs149201802(G,T;G,T)
Reference rs149201802(C;C)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome Tumor susceptibility linked to germline BAP1 mutations
Variation info
Gene RAD50
CLNDBN Hereditary cancer-predisposing syndrome Tumor susceptibility linked to germline BAP1 mutations
Reversed 0
HGVS NC_000005.9:g.131930642C>G; NC_000005.9:g.131930642C>T
CLNSRC
CLNACC RCV000205188.2, RCV000219115.1, RCV000163046.3,