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rs876659005

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs876659005(-;-)
Make rs876659005(-;A)
Make rs876659005(A;A)
ReferenceGRCh38.p2 38.2/147
Chromosome5
Position132579871
GeneRAD50
is asnp
is mentioned by
dbSNPrs876659005
ebirs876659005
HLIrs876659005
Exacrs876659005
Varsomers876659005
Maprs876659005
PheGenIrs876659005
hapmaprs876659005
1000 genomesrs876659005
hgdprs876659005
ensemblrs876659005
gopubmedrs876659005
geneviewrs876659005
scholarrs876659005
googlers876659005
pharmgkbrs876659005
gwascentralrs876659005
openSNPrs876659005
23andMers876659005
23andMe allrs876659005
SNP Nexus

SNPshotrs876659005
SNPdbers876659005
MSV3drs876659005
GWAS Ctlgrs876659005
Max Magnitude0
ClinVar
Risk rs876659005(A;A)
Alt rs876659005(A;A)
Reference rs876659005(;)
Significance Pathogenic
Disease Tumor susceptibility linked to germline BAP1 mutations Hereditary cancer-predisposing syndrome
Variation info
Gene RAD50
CLNDBN Tumor susceptibility linked to germline BAP1 mutations Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000005.9:g.131915563dupA
CLNSRC
CLNACC RCV000220809.1, RCV000226081.1,