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rs786204751

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs786204751(C;T)
Make rs786204751(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome11
Position108304693
GeneATM
is asnp
is mentioned by
dbSNPrs786204751
ebirs786204751
HLIrs786204751
Exacrs786204751
Varsomers786204751
Maprs786204751
PheGenIrs786204751
hapmaprs786204751
1000 genomesrs786204751
hgdprs786204751
ensemblrs786204751
gopubmedrs786204751
geneviewrs786204751
scholarrs786204751
googlers786204751
pharmgkbrs786204751
gwascentralrs786204751
openSNPrs786204751
23andMers786204751
23andMe allrs786204751
SNP Nexus

SNPshotrs786204751
SNPdbers786204751
MSV3drs786204751
GWAS Ctlgrs786204751
Max Magnitude0
ClinVar
Risk rs786204751(T;T)
Alt rs786204751(T;T)
Reference rs786204751(C;C)
Significance Probable-Pathogenic
Disease Ataxia-telangiectasia syndrome
Variation info
Gene ATM
CLNDBN Ataxia-telangiectasia syndrome
Reversed 0
HGVS NC_000011.9:g.108175420C>T
CLNSRC
CLNACC RCV000169605.1,