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rs786202801

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs786202801(A;A)
Make rs786202801(A;T)
ReferenceGRCh38.p2 38.2/146
Chromosome11
Position94429909
GeneMRE11A
is asnp
is mentioned by
dbSNPrs786202801
ebirs786202801
HLIrs786202801
Exacrs786202801
Varsomers786202801
Maprs786202801
PheGenIrs786202801
hapmaprs786202801
1000 genomesrs786202801
hgdprs786202801
ensemblrs786202801
gopubmedrs786202801
geneviewrs786202801
scholarrs786202801
googlers786202801
pharmgkbrs786202801
gwascentralrs786202801
openSNPrs786202801
23andMers786202801
23andMe allrs786202801
SNP Nexus

SNPshotrs786202801
SNPdbers786202801
MSV3drs786202801
GWAS Ctlgrs786202801
Max Magnitude0
ClinVar
Risk rs786202801(A;A)
Alt rs786202801(A;A)
Reference rs786202801(T;T)
Significance Probable-Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene MRE11A
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 1
HGVS NC_000011.9:g.94163075A>T
CLNSRC Western University
CLNACC RCV000165802.1,