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rs876660186

From SNPedia

Orientationminus
Geno Mag Summary
(CTTATGAG;CTTATGAG) 0 common in clinvar
Make rs876660186(-;-)
Make rs876660186(-;CTTATGAG)
ReferenceGRCh38.p2 38.2/147
Chromosome11
Position94447362
GeneMRE11
is asnp
is mentioned by
dbSNPrs876660186
ebirs876660186
HLIrs876660186
Exacrs876660186
Varsomers876660186
Maprs876660186
PheGenIrs876660186
hapmaprs876660186
1000 genomesrs876660186
hgdprs876660186
ensemblrs876660186
gopubmedrs876660186
geneviewrs876660186
scholarrs876660186
googlers876660186
pharmgkbrs876660186
gwascentralrs876660186
openSNPrs876660186
23andMers876660186
23andMe allrs876660186
SNP Nexus

SNPshotrs876660186
SNPdbers876660186
MSV3drs876660186
GWAS Ctlgrs876660186
Max Magnitude0
ClinVar
Risk rs876660186(;)
Alt rs876660186(;)
Reference rs876660186(CTTATGAG;CTTATGAG)
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.94180528_94180535delCTCATAAG
CLNSRC
CLNACC RCV000218839.1,