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rs786202253

From SNPedia

Orientationminus
Geno Mag Summary
(GCTTCAAA;GCTTCAAA) 0 common in clinvar
Make rs786202253(-;-)
Make rs786202253(-;GCTTCAAA)
ReferenceGRCh38.p2 38.2/146
Chromosome11
Position94478768
GeneMRE11A
is asnp
is mentioned by
dbSNPrs786202253
ebirs786202253
HLIrs786202253
Exacrs786202253
Varsomers786202253
Maprs786202253
PheGenIrs786202253
hapmaprs786202253
1000 genomesrs786202253
hgdprs786202253
ensemblrs786202253
gopubmedrs786202253
geneviewrs786202253
scholarrs786202253
googlers786202253
pharmgkbrs786202253
gwascentralrs786202253
openSNPrs786202253
23andMers786202253
23andMe allrs786202253
SNP Nexus

SNPshotrs786202253
SNPdbers786202253
MSV3drs786202253
GWAS Ctlgrs786202253
Max Magnitude0
ClinVar
Risk rs786202253(;)
Alt rs786202253(;)
Reference rs786202253(GCTTCAAA;GCTTCAAA)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene MRE11A
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 1
HGVS NC_000011.9:g.94211934_94211941delTTTGAAGC
CLNSRC
CLNACC RCV000164971.1,