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rs876659145

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs876659145(A;G)
Make rs876659145(G;G)
ReferenceGRCh38.p2 38.2/147
Chromosome11
Position94479763
GeneMRE11
is asnp
is mentioned by
dbSNPrs876659145
ebirs876659145
HLIrs876659145
Exacrs876659145
Varsomers876659145
Maprs876659145
PheGenIrs876659145
hapmaprs876659145
1000 genomesrs876659145
hgdprs876659145
ensemblrs876659145
gopubmedrs876659145
geneviewrs876659145
scholarrs876659145
googlers876659145
pharmgkbrs876659145
gwascentralrs876659145
openSNPrs876659145
23andMers876659145
23andMe allrs876659145
SNP Nexus

SNPshotrs876659145
SNPdbers876659145
MSV3drs876659145
GWAS Ctlgrs876659145
Max Magnitude0
ClinVar
Risk rs876659145(G;G)
Alt rs876659145(G;G)
Reference rs876659145(A;A)
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.94212929T>C
CLNSRC
CLNACC RCV000215862.1,