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rs371077728

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs371077728(A;A)
Make rs371077728(A;G)
ReferenceGRCh38 38.1/142
Chromosome11
Position94467821
GeneMIR548L, MRE11A
is asnp
is mentioned by
dbSNPrs371077728
ebirs371077728
HLIrs371077728
Exacrs371077728
Varsomers371077728
Maprs371077728
PheGenIrs371077728
hapmaprs371077728
1000 genomesrs371077728
hgdprs371077728
ensemblrs371077728
gopubmedrs371077728
geneviewrs371077728
scholarrs371077728
googlers371077728
pharmgkbrs371077728
gwascentralrs371077728
openSNPrs371077728
23andMers371077728
23andMe allrs371077728
SNP Nexus

SNPshotrs371077728
SNPdbers371077728
MSV3drs371077728
GWAS Ctlgrs371077728
Max Magnitude0
ClinVar
Risk rs371077728(A,C,T;A,C,T)
Alt rs371077728(A,C,T;A,C,T)
Reference rs371077728(G;G)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome not specified Tumor susceptibility linked to germline BAP1 mutations
Variation info
Gene MIR548L MRE11A
CLNDBN Hereditary cancer-predisposing syndrome not specified Tumor susceptibility linked to germline BAP1 mutations
Reversed 0
HGVS NC_000011.9:g.94200987G>A; NC_000011.9:g.94200987G>C; NC_000011.9:g.94200987G>T
CLNSRC Ambry Genetics ClinVar GeneDx
CLNACC RCV000129234.3, RCV000115902.2, RCV000220133.1, RCV000166423.1,