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rs786203008

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs786203008(-;-)
Make rs786203008(-;T)
ReferenceGRCh38.p2 38.2/146
Chromosome11
Position108317402
GeneATM
is asnp
is mentioned by
dbSNPrs786203008
ebirs786203008
HLIrs786203008
Exacrs786203008
Varsomers786203008
Maprs786203008
PheGenIrs786203008
hapmaprs786203008
1000 genomesrs786203008
hgdprs786203008
ensemblrs786203008
gopubmedrs786203008
geneviewrs786203008
scholarrs786203008
googlers786203008
pharmgkbrs786203008
gwascentralrs786203008
openSNPrs786203008
23andMers786203008
23andMe allrs786203008
SNP Nexus

SNPshotrs786203008
SNPdbers786203008
MSV3drs786203008
GWAS Ctlgrs786203008
Max Magnitude0
ClinVar
Risk rs786203008(;)
Alt rs786203008(;)
Reference rs786203008(T;T)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome Ataxia-telangiectasia syndrome not provided
Variation info
Gene C11orf65 ATM
CLNDBN Hereditary cancer-predisposing syndrome Ataxia-telangiectasia syndrome not provided
Reversed 0
HGVS NC_000011.9:g.108188129delT
CLNSRC
CLNACC RCV000166124.1, RCV000205743.1, RCV000236779.1,