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rs786201693

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs786201693(C;G)
Make rs786201693(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome11
Position108243969
GeneATM
is asnp
is mentioned by
dbSNPrs786201693
ebirs786201693
HLIrs786201693
Exacrs786201693
Varsomers786201693
Maprs786201693
PheGenIrs786201693
hapmaprs786201693
1000 genomesrs786201693
hgdprs786201693
ensemblrs786201693
gopubmedrs786201693
geneviewrs786201693
scholarrs786201693
googlers786201693
pharmgkbrs786201693
gwascentralrs786201693
openSNPrs786201693
23andMers786201693
23andMe allrs786201693
SNP Nexus

SNPshotrs786201693
SNPdbers786201693
MSV3drs786201693
GWAS Ctlgrs786201693
Max Magnitude0
ClinVar
Risk rs786201693(G;G)
Alt rs786201693(G;G)
Reference rs786201693(C;C)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene ATM
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000011.9:g.108114696C>G
CLNSRC
CLNACC RCV000164103.1,