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rs786202608

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs786202608(-;-)
Make rs786202608(-;T)
ReferenceGRCh38.p2 38.2/146
Chromosome11
Position108268525
GeneATM
is asnp
is mentioned by
dbSNPrs786202608
ebirs786202608
HLIrs786202608
Exacrs786202608
Varsomers786202608
Maprs786202608
PheGenIrs786202608
hapmaprs786202608
1000 genomesrs786202608
hgdprs786202608
ensemblrs786202608
gopubmedrs786202608
geneviewrs786202608
scholarrs786202608
googlers786202608
pharmgkbrs786202608
gwascentralrs786202608
openSNPrs786202608
23andMers786202608
23andMe allrs786202608
SNP Nexus

SNPshotrs786202608
SNPdbers786202608
MSV3drs786202608
GWAS Ctlgrs786202608
Max Magnitude0
ClinVar
Risk rs786202608(;)
Alt rs786202608(;)
Reference rs786202608(T;T)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene ATM
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000011.9:g.108139252delT
CLNSRC
CLNACC RCV000165502.1,