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rs876659255

From SNPedia

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Geno Mag Summary
(TC;TC) 0 common in clinvar
Make rs876659255(A;A)
Make rs876659255(A;TC)
ReferenceGRCh38.p2 38.2/147
Chromosome5
Position132579492
GeneRAD50
is asnp
is mentioned by
dbSNPrs876659255
ebirs876659255
HLIrs876659255
Exacrs876659255
Varsomers876659255
Maprs876659255
PheGenIrs876659255
hapmaprs876659255
1000 genomesrs876659255
hgdprs876659255
ensemblrs876659255
gopubmedrs876659255
geneviewrs876659255
scholarrs876659255
googlers876659255
pharmgkbrs876659255
gwascentralrs876659255
openSNPrs876659255
23andMers876659255
23andMe allrs876659255
SNP Nexus

SNPshotrs876659255
SNPdbers876659255
MSV3drs876659255
GWAS Ctlgrs876659255
Max Magnitude0
ClinVar
Risk rs876659255(A;A)
Alt rs876659255(A;A)
Reference rs876659255(TC;TC)
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.131915184_131915185delTCinsA
CLNSRC
CLNACC RCV000215584.1,