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rs876658665

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs876658665(A;A)
Make rs876658665(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome11
Position94464112
GeneMRE11
is asnp
is mentioned by
dbSNPrs876658665
ebirs876658665
HLIrs876658665
Exacrs876658665
Varsomers876658665
Maprs876658665
PheGenIrs876658665
hapmaprs876658665
1000 genomesrs876658665
hgdprs876658665
ensemblrs876658665
gopubmedrs876658665
geneviewrs876658665
scholarrs876658665
googlers876658665
pharmgkbrs876658665
gwascentralrs876658665
openSNPrs876658665
23andMers876658665
23andMe allrs876658665
SNP Nexus

SNPshotrs876658665
SNPdbers876658665
MSV3drs876658665
GWAS Ctlgrs876658665
Max Magnitude0
ClinVar
Risk rs876658665(A;A)
Alt rs876658665(A;A)
Reference rs876658665(G;G)
Significance Probable-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.94197278C>T
CLNSRC
CLNACC RCV000214897.1,