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rs786201689

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs786201689(A;A)
Make rs786201689(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome11
Position108251966
GeneATM
is asnp
is mentioned by
dbSNPrs786201689
ebirs786201689
HLIrs786201689
Exacrs786201689
Varsomers786201689
Maprs786201689
PheGenIrs786201689
hapmaprs786201689
1000 genomesrs786201689
hgdprs786201689
ensemblrs786201689
gopubmedrs786201689
geneviewrs786201689
scholarrs786201689
googlers786201689
pharmgkbrs786201689
gwascentralrs786201689
openSNPrs786201689
23andMers786201689
23andMe allrs786201689
SNP Nexus

SNPshotrs786201689
SNPdbers786201689
MSV3drs786201689
GWAS Ctlgrs786201689
Max Magnitude0
ClinVar
Risk rs786201689(A;A)
Alt rs786201689(A;A)
Reference rs786201689(G;G)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene ATM
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000011.9:g.108122693G>A
CLNSRC
CLNACC RCV000164097.1,