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rs759130031

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs759130031(C;T)
Make rs759130031(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome11
Position94476288
GeneMRE11
is asnp
is mentioned by
dbSNPrs759130031
ebirs759130031
HLIrs759130031
Exacrs759130031
Varsomers759130031
Maprs759130031
PheGenIrs759130031
hapmaprs759130031
1000 genomesrs759130031
hgdprs759130031
ensemblrs759130031
gopubmedrs759130031
geneviewrs759130031
scholarrs759130031
googlers759130031
pharmgkbrs759130031
gwascentralrs759130031
openSNPrs759130031
23andMers759130031
23andMe allrs759130031
SNP Nexus

SNPshotrs759130031
SNPdbers759130031
MSV3drs759130031
GWAS Ctlgrs759130031
Max Magnitude0
ClinVar
Risk rs759130031(T;T)
Alt rs759130031(T;T)
Reference rs759130031(C;C)
Significance Pathogenic
Disease Tumor susceptibility linked to germline BAP1 mutations
Variation info
Gene MRE11A
CLNDBN Tumor susceptibility linked to germline BAP1 mutations
Reversed 0
HGVS NC_000011.9:g.94209454C>T
CLNSRC
CLNACC RCV000217276.1,