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rs876659343

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs876659343(C;C)
Make rs876659343(C;T)
ReferenceGRCh38.p2 38.2/147
Chromosome11
Position94467811
GeneMIR548L, MRE11
is asnp
is mentioned by
dbSNPrs876659343
ebirs876659343
HLIrs876659343
Exacrs876659343
Varsomers876659343
Maprs876659343
PheGenIrs876659343
hapmaprs876659343
1000 genomesrs876659343
hgdprs876659343
ensemblrs876659343
gopubmedrs876659343
geneviewrs876659343
scholarrs876659343
googlers876659343
pharmgkbrs876659343
gwascentralrs876659343
openSNPrs876659343
23andMers876659343
23andMe allrs876659343
SNP Nexus

SNPshotrs876659343
SNPdbers876659343
MSV3drs876659343
GWAS Ctlgrs876659343
Max Magnitude0
ClinVar
Risk rs876659343(C;C)
Alt rs876659343(C;C)
Reference rs876659343(T;T)
Significance Probable-Pathogenic
Disease Tumor susceptibility linked to germline BAP1 mutations
Variation info
Gene MIR548L MRE11A
CLNDBN Tumor susceptibility linked to germline BAP1 mutations
Reversed 1
HGVS NC_000011.9:g.94200977A>G
CLNSRC
CLNACC RCV000221914.1,