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rs786202264

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(ATGAAAGTCTCAA;ATGAAAGTCTCAA) 0 common in clinvar
Make rs786202264(-;-)
Make rs786202264(-;GAAAGTCTCAAAT)
Make rs786202264(GAAAGTCTCAAAT;GAAAGTCTCAAAT)
ReferenceGRCh38.p2 38.2/146
Chromosome11
Position108320039
GeneATM, C11orf65
is asnp
is mentioned by
dbSNPrs786202264
dbSNP (old)rs786202264
ClinGenrs786202264
ebirs786202264
HLIrs786202264
Exacrs786202264
Gnomadrs786202264
Varsomers786202264
Maprs786202264
PheGenIrs786202264
Biobankrs786202264
1000 genomesrs786202264
hgdprs786202264
ensemblrs786202264
gopubmedrs786202264
geneviewrs786202264
scholarrs786202264
googlers786202264
pharmgkbrs786202264
gwascentralrs786202264
openSNPrs786202264
23andMers786202264
23andMe allrs786202264
SNP Nexus

SNPshotrs786202264
SNPdbers786202264
MSV3drs786202264
GWAS Ctlgrs786202264
Max Magnitude0
ClinVar
Risk rs786202264(-;-)
Alt rs786202264(-;-)
Reference Rs786202264(ATGAAAGTCTCAA;ATGAAAGTCTCAA)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene C11orf65 ATM
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000011.9:g.108190766_108190778delGAAAGTCTCAAAT
CLNSRC
CLNACC RCV000164992.1,