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rs776912688

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs776912688(A;A)
Make rs776912688(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome11
Position94471613
GeneMRE11
is asnp
is mentioned by
dbSNPrs776912688
ebirs776912688
HLIrs776912688
Exacrs776912688
Varsomers776912688
Maprs776912688
PheGenIrs776912688
hapmaprs776912688
1000 genomesrs776912688
hgdprs776912688
ensemblrs776912688
gopubmedrs776912688
geneviewrs776912688
scholarrs776912688
googlers776912688
pharmgkbrs776912688
gwascentralrs776912688
openSNPrs776912688
23andMers776912688
23andMe allrs776912688
SNP Nexus

SNPshotrs776912688
SNPdbers776912688
MSV3drs776912688
GWAS Ctlgrs776912688
Max Magnitude0
ClinVar
Risk rs776912688(A;A)
Alt rs776912688(A;A)
Reference rs776912688(G;G)
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.94204779G>C
CLNSRC
CLNACC RCV000219565.1,