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rs876660364

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs876660364(A;T)
Make rs876660364(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome5
Position132609340
GeneRAD50
is asnp
is mentioned by
dbSNPrs876660364
ebirs876660364
HLIrs876660364
Exacrs876660364
Varsomers876660364
Maprs876660364
PheGenIrs876660364
hapmaprs876660364
1000 genomesrs876660364
hgdprs876660364
ensemblrs876660364
gopubmedrs876660364
geneviewrs876660364
scholarrs876660364
googlers876660364
pharmgkbrs876660364
gwascentralrs876660364
openSNPrs876660364
23andMers876660364
23andMe allrs876660364
SNP Nexus

SNPshotrs876660364
SNPdbers876660364
MSV3drs876660364
GWAS Ctlgrs876660364
Max Magnitude0
ClinVar
Risk rs876660364(T;T)
Alt rs876660364(T;T)
Reference rs876660364(A;A)
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.131945032A>T
CLNSRC
CLNACC RCV000213422.1,