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rs876660957

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs876660957(A;C)
Make rs876660957(C;C)
ReferenceGRCh38.p2 38.2/147
Chromosome5
Position132588685
GeneRAD50
is asnp
is mentioned by
dbSNPrs876660957
ebirs876660957
HLIrs876660957
Exacrs876660957
Varsomers876660957
Maprs876660957
PheGenIrs876660957
hapmaprs876660957
1000 genomesrs876660957
hgdprs876660957
ensemblrs876660957
gopubmedrs876660957
geneviewrs876660957
scholarrs876660957
googlers876660957
pharmgkbrs876660957
gwascentralrs876660957
openSNPrs876660957
23andMers876660957
23andMe allrs876660957
SNP Nexus

SNPshotrs876660957
SNPdbers876660957
MSV3drs876660957
GWAS Ctlgrs876660957
Max Magnitude0
ClinVar
Risk rs876660957(C;C)
Alt rs876660957(C;C)
Reference rs876660957(A;A)
Significance Probable-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.131924377A>C
CLNSRC
CLNACC RCV000222834.1,