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rs761168506

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs761168506(C;C)
Make rs761168506(C;T)
ReferenceGRCh38.p2 38.2/147
Chromosome5
Position132637202
GeneRAD50, TH2LCRR
is asnp
is mentioned by
dbSNPrs761168506
ebirs761168506
HLIrs761168506
Exacrs761168506
Varsomers761168506
Maprs761168506
PheGenIrs761168506
hapmaprs761168506
1000 genomesrs761168506
hgdprs761168506
ensemblrs761168506
gopubmedrs761168506
geneviewrs761168506
scholarrs761168506
googlers761168506
pharmgkbrs761168506
gwascentralrs761168506
openSNPrs761168506
23andMers761168506
23andMe allrs761168506
SNP Nexus

SNPshotrs761168506
SNPdbers761168506
MSV3drs761168506
GWAS Ctlgrs761168506
Max Magnitude0
ClinVar
Risk rs761168506(C;C)
Alt rs761168506(C;C)
Reference rs761168506(T;T)
Significance Probable-Pathogenic
Disease Tumor susceptibility linked to germline BAP1 mutations
Variation info
Gene TH2LCRR RAD50
CLNDBN Tumor susceptibility linked to germline BAP1 mutations
Reversed 0
HGVS NC_000005.9:g.131972894T>C
CLNSRC
CLNACC RCV000223053.1,