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rs876660160

From SNPedia

Orientationplus
Geno Mag Summary
(GA;GA) 0 common in clinvar
Make rs876660160(-;-)
Make rs876660160(-;GA)
ReferenceGRCh38.p2 38.2/147
Chromosome5
Position132588803
GeneRAD50
is asnp
is mentioned by
dbSNPrs876660160
ebirs876660160
HLIrs876660160
Exacrs876660160
Varsomers876660160
Maprs876660160
PheGenIrs876660160
hapmaprs876660160
1000 genomesrs876660160
hgdprs876660160
ensemblrs876660160
gopubmedrs876660160
geneviewrs876660160
scholarrs876660160
googlers876660160
pharmgkbrs876660160
gwascentralrs876660160
openSNPrs876660160
23andMers876660160
23andMe allrs876660160
SNP Nexus

SNPshotrs876660160
SNPdbers876660160
MSV3drs876660160
GWAS Ctlgrs876660160
Max Magnitude0
ClinVar
Risk rs876660160(;)
Alt rs876660160(;)
Reference rs876660160(GA;GA)
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.131924495_131924496delGA
CLNSRC
CLNACC RCV000223038.1,