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rs786201886

From SNPedia

Orientationplus
Geno Mag Summary
(TAT;TAT) 0 common in clinvar
Make rs786201886(CA;CA)
Make rs786201886(CA;TAT)
ReferenceGRCh38.p2 38.2/146
Chromosome11
Position108284234
GeneATM
is asnp
is mentioned by
dbSNPrs786201886
ebirs786201886
HLIrs786201886
Exacrs786201886
Varsomers786201886
Maprs786201886
PheGenIrs786201886
hapmaprs786201886
1000 genomesrs786201886
hgdprs786201886
ensemblrs786201886
gopubmedrs786201886
geneviewrs786201886
scholarrs786201886
googlers786201886
pharmgkbrs786201886
gwascentralrs786201886
openSNPrs786201886
23andMers786201886
23andMe allrs786201886
SNP Nexus

SNPshotrs786201886
SNPdbers786201886
MSV3drs786201886
GWAS Ctlgrs786201886
Max Magnitude0
ClinVar
Risk rs786201886(CA;CA)
Alt rs786201886(CA;CA)
Reference rs786201886(TAT;TAT)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene ATM
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000011.9:g.108154961_108154963delTATinsCA
CLNSRC
CLNACC RCV000164396.1,