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rs876659654

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs876659654(C;T)
Make rs876659654(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome5
Position132642212
GeneRAD50, TH2LCRR
is asnp
is mentioned by
dbSNPrs876659654
ebirs876659654
HLIrs876659654
Exacrs876659654
Varsomers876659654
Maprs876659654
PheGenIrs876659654
hapmaprs876659654
1000 genomesrs876659654
hgdprs876659654
ensemblrs876659654
gopubmedrs876659654
geneviewrs876659654
scholarrs876659654
googlers876659654
pharmgkbrs876659654
gwascentralrs876659654
openSNPrs876659654
23andMers876659654
23andMe allrs876659654
SNP Nexus

SNPshotrs876659654
SNPdbers876659654
MSV3drs876659654
GWAS Ctlgrs876659654
Max Magnitude0
ClinVar
Risk rs876659654(T;T)
Alt rs876659654(T;T)
Reference rs876659654(C;C)
Significance Pathogenic
Disease Tumor susceptibility linked to germline BAP1 mutations
Variation info
Gene LOC101927761 TH2LCRR RAD50
CLNDBN Tumor susceptibility linked to germline BAP1 mutations
Reversed 0
HGVS NC_000005.9:g.131977904C>T
CLNSRC
CLNACC RCV000222239.1,