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rs786202474

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs786202474(-;-)
Make rs786202474(-;T)
Make rs786202474(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome11
Position108252894
GeneATM
is asnp
is mentioned by
dbSNPrs786202474
ebirs786202474
HLIrs786202474
Exacrs786202474
Varsomers786202474
Maprs786202474
PheGenIrs786202474
hapmaprs786202474
1000 genomesrs786202474
hgdprs786202474
ensemblrs786202474
gopubmedrs786202474
geneviewrs786202474
scholarrs786202474
googlers786202474
pharmgkbrs786202474
gwascentralrs786202474
openSNPrs786202474
23andMers786202474
23andMe allrs786202474
SNP Nexus

SNPshotrs786202474
SNPdbers786202474
MSV3drs786202474
GWAS Ctlgrs786202474
Max Magnitude0
ClinVar
Risk rs786202474(T;T)
Alt rs786202474(T;T)
Reference rs786202474(;)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene ATM
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000011.9:g.108123621dupT
CLNSRC
CLNACC RCV000165300.1,