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rs876660269

From SNPedia

Orientationminus
Geno Mag Summary
(;) 0 common in clinvar
Make rs876660269(-;-)
Make rs876660269(-;A)
Make rs876660269(A;A)
ReferenceGRCh38.p2 38.2/147
Chromosome11
Position94445850
GeneMRE11
is asnp
is mentioned by
dbSNPrs876660269
ebirs876660269
HLIrs876660269
Exacrs876660269
Varsomers876660269
Maprs876660269
PheGenIrs876660269
hapmaprs876660269
1000 genomesrs876660269
hgdprs876660269
ensemblrs876660269
gopubmedrs876660269
geneviewrs876660269
scholarrs876660269
googlers876660269
pharmgkbrs876660269
gwascentralrs876660269
openSNPrs876660269
23andMers876660269
23andMe allrs876660269
SNP Nexus

SNPshotrs876660269
SNPdbers876660269
MSV3drs876660269
GWAS Ctlgrs876660269
Max Magnitude0
ClinVar
Risk rs876660269(A;A)
Alt rs876660269(A;A)
Reference rs876660269(;)
Significance Pathogenic
Disease Tumor susceptibility linked to germline BAP1 mutations
Variation info
Gene MRE11A
CLNDBN Tumor susceptibility linked to germline BAP1 mutations
Reversed 1
HGVS NC_000011.9:g.94179017dupT
CLNSRC
CLNACC RCV000218130.1,