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rs876659837

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs876659837(-;-)
Make rs876659837(-;A)
ReferenceGRCh38.p2 38.2/147
Chromosome5
Position132559308
GeneRAD50
is asnp
is mentioned by
dbSNPrs876659837
ebirs876659837
HLIrs876659837
Exacrs876659837
Varsomers876659837
Maprs876659837
PheGenIrs876659837
hapmaprs876659837
1000 genomesrs876659837
hgdprs876659837
ensemblrs876659837
gopubmedrs876659837
geneviewrs876659837
scholarrs876659837
googlers876659837
pharmgkbrs876659837
gwascentralrs876659837
openSNPrs876659837
23andMers876659837
23andMe allrs876659837
SNP Nexus

SNPshotrs876659837
SNPdbers876659837
MSV3drs876659837
GWAS Ctlgrs876659837
Max Magnitude0
ClinVar
Risk rs876659837(;)
Alt rs876659837(;)
Reference rs876659837(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.131895000delA
CLNSRC
CLNACC RCV000220905.1,