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rs876660039

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs876660039(-;-)
Make rs876660039(-;C)
ReferenceGRCh38.p2 38.2/147
Chromosome5
Position132588809
GeneRAD50
is asnp
is mentioned by
dbSNPrs876660039
ebirs876660039
HLIrs876660039
Exacrs876660039
Varsomers876660039
Maprs876660039
PheGenIrs876660039
hapmaprs876660039
1000 genomesrs876660039
hgdprs876660039
ensemblrs876660039
gopubmedrs876660039
geneviewrs876660039
scholarrs876660039
googlers876660039
pharmgkbrs876660039
gwascentralrs876660039
openSNPrs876660039
23andMers876660039
23andMe allrs876660039
SNP Nexus

SNPshotrs876660039
SNPdbers876660039
MSV3drs876660039
GWAS Ctlgrs876660039
Max Magnitude0
ClinVar
Risk rs876660039(;)
Alt rs876660039(;)
Reference rs876660039(C;C)
Significance Pathogenic
Disease Tumor susceptibility linked to germline BAP1 mutations
Variation info
Gene RAD50
CLNDBN Tumor susceptibility linked to germline BAP1 mutations
Reversed 0
HGVS NC_000005.9:g.131924501delC
CLNSRC
CLNACC RCV000214856.1,