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rs1799757

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs1799757(-;-)
Make rs1799757(-;T)
ReferenceGRCh38.p2 38.2/146
Chromosome11
Position108279481
GeneATM
is asnp
is mentioned by
dbSNPrs1799757
ebirs1799757
HLIrs1799757
Exacrs1799757
Varsomers1799757
Maprs1799757
PheGenIrs1799757
hapmaprs1799757
1000 genomesrs1799757
hgdprs1799757
ensemblrs1799757
gopubmedrs1799757
geneviewrs1799757
scholarrs1799757
googlers1799757
pharmgkbrs1799757
gwascentralrs1799757
openSNPrs1799757
23andMers1799757
23andMe allrs1799757
SNP Nexus

SNPshotrs1799757
SNPdbers1799757
MSV3drs1799757
GWAS Ctlgrs1799757
Merged fromRs3218698
Max Magnitude0
ClinVar
Risk rs1799757(;)
Alt rs1799757(;)
Reference rs1799757(T;T)
Significance Non-pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene ATM
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000011.9:g.108150209delT
CLNSRC
CLNACC RCV000159613.2,