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rs786201957

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs786201957(C;T)
Make rs786201957(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome11
Position108279555
GeneATM
is asnp
is mentioned by
dbSNPrs786201957
ebirs786201957
HLIrs786201957
Exacrs786201957
Varsomers786201957
Maprs786201957
PheGenIrs786201957
hapmaprs786201957
1000 genomesrs786201957
hgdprs786201957
ensemblrs786201957
gopubmedrs786201957
geneviewrs786201957
scholarrs786201957
googlers786201957
pharmgkbrs786201957
gwascentralrs786201957
openSNPrs786201957
23andMers786201957
23andMe allrs786201957
SNP Nexus

SNPshotrs786201957
SNPdbers786201957
MSV3drs786201957
GWAS Ctlgrs786201957
Max Magnitude0
ClinVar
Risk rs786201957(T;T)
Alt rs786201957(T;T)
Reference Rs786201957(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.108150282C>T
CLNSRC
CLNACC RCV000164505.1,