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rs786203166

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs786203166(-;-)
Make rs786203166(-;A)
ReferenceGRCh38.p2 38.2/146
Chromosome11
Position108250714
GeneATM
is asnp
is mentioned by
dbSNPrs786203166
ebirs786203166
HLIrs786203166
Exacrs786203166
Varsomers786203166
Maprs786203166
PheGenIrs786203166
hapmaprs786203166
1000 genomesrs786203166
hgdprs786203166
ensemblrs786203166
gopubmedrs786203166
geneviewrs786203166
scholarrs786203166
googlers786203166
pharmgkbrs786203166
gwascentralrs786203166
openSNPrs786203166
23andMers786203166
23andMe allrs786203166
SNP Nexus

SNPshotrs786203166
SNPdbers786203166
MSV3drs786203166
GWAS Ctlgrs786203166
Max Magnitude0
ClinVar
Risk rs786203166(;)
Alt rs786203166(;)
Reference rs786203166(A;A)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene ATM
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000011.9:g.108121441delA
CLNSRC
CLNACC RCV000166356.1,