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rs786202783

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs786202783(-;-)
Make rs786202783(-;G)
ReferenceGRCh38.p2 38.2/146
Chromosome11
Position108259076
GeneATM
is asnp
is mentioned by
dbSNPrs786202783
ebirs786202783
HLIrs786202783
Exacrs786202783
Varsomers786202783
Maprs786202783
PheGenIrs786202783
hapmaprs786202783
1000 genomesrs786202783
hgdprs786202783
ensemblrs786202783
gopubmedrs786202783
geneviewrs786202783
scholarrs786202783
googlers786202783
pharmgkbrs786202783
gwascentralrs786202783
openSNPrs786202783
23andMers786202783
23andMe allrs786202783
SNP Nexus

SNPshotrs786202783
SNPdbers786202783
MSV3drs786202783
GWAS Ctlgrs786202783
Max Magnitude0
ClinVar
Risk rs786202783(;)
Alt rs786202783(;)
Reference rs786202783(G;G)
Significance Probable-Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene ATM
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000011.9:g.108129803delG
CLNSRC
CLNACC RCV000165770.1,