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rs786203796

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs786203796(A;G)
Make rs786203796(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome11
Position108304673
GeneATM
is asnp
is mentioned by
dbSNPrs786203796
ebirs786203796
HLIrs786203796
Exacrs786203796
Varsomers786203796
Maprs786203796
PheGenIrs786203796
hapmaprs786203796
1000 genomesrs786203796
hgdprs786203796
ensemblrs786203796
gopubmedrs786203796
geneviewrs786203796
scholarrs786203796
googlers786203796
pharmgkbrs786203796
gwascentralrs786203796
openSNPrs786203796
23andMers786203796
23andMe allrs786203796
SNP Nexus

SNPshotrs786203796
SNPdbers786203796
MSV3drs786203796
GWAS Ctlgrs786203796
Max Magnitude0
ClinVar
Risk rs786203796(G;G)
Alt rs786203796(G;G)
Reference rs786203796(A;A)
Significance Probable-Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene ATM
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000011.9:g.108175400A>G
CLNSRC
CLNACC RCV000167256.1,