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rs786202323

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs786202323(-;-)
Make rs786202323(-;A)
Make rs786202323(A;A)
ReferenceGRCh38.p2 38.2/146
Chromosome11
Position108320042
GeneATM
is asnp
is mentioned by
dbSNPrs786202323
ebirs786202323
HLIrs786202323
Exacrs786202323
Varsomers786202323
Maprs786202323
PheGenIrs786202323
hapmaprs786202323
1000 genomesrs786202323
hgdprs786202323
ensemblrs786202323
gopubmedrs786202323
geneviewrs786202323
scholarrs786202323
googlers786202323
pharmgkbrs786202323
gwascentralrs786202323
openSNPrs786202323
23andMers786202323
23andMe allrs786202323
SNP Nexus

SNPshotrs786202323
SNPdbers786202323
MSV3drs786202323
GWAS Ctlgrs786202323
Max Magnitude0
ClinVar
Risk rs786202323(A;A)
Alt rs786202323(A;A)
Reference rs786202323(;)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene C11orf65 ATM
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000011.9:g.108190769dupA
CLNSRC
CLNACC RCV000165073.1,