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rs786202694

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs786202694(-;-)
Make rs786202694(-;G)
Make rs786202694(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome11
Position108284260
GeneATM
is asnp
is mentioned by
dbSNPrs786202694
ebirs786202694
HLIrs786202694
Exacrs786202694
Varsomers786202694
Maprs786202694
PheGenIrs786202694
hapmaprs786202694
1000 genomesrs786202694
hgdprs786202694
ensemblrs786202694
gopubmedrs786202694
geneviewrs786202694
scholarrs786202694
googlers786202694
pharmgkbrs786202694
gwascentralrs786202694
openSNPrs786202694
23andMers786202694
23andMe allrs786202694
SNP Nexus

SNPshotrs786202694
SNPdbers786202694
MSV3drs786202694
GWAS Ctlgrs786202694
Max Magnitude0
ClinVar
Risk rs786202694(G;G)
Alt rs786202694(G;G)
Reference rs786202694(;)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene ATM
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000011.9:g.108154987dupG
CLNSRC
CLNACC RCV000165632.1,