Have questions? Visit https://www.reddit.com/r/SNPedia

rs786202350

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs786202350(-;-)
Make rs786202350(-;T)
ReferenceGRCh38.p2 38.2/146
Chromosome11
Position108287658
GeneATM
is asnp
is mentioned by
dbSNPrs786202350
ebirs786202350
HLIrs786202350
Exacrs786202350
Varsomers786202350
Maprs786202350
PheGenIrs786202350
hapmaprs786202350
1000 genomesrs786202350
hgdprs786202350
ensemblrs786202350
gopubmedrs786202350
geneviewrs786202350
scholarrs786202350
googlers786202350
pharmgkbrs786202350
gwascentralrs786202350
openSNPrs786202350
23andMers786202350
23andMe allrs786202350
SNP Nexus

SNPshotrs786202350
SNPdbers786202350
MSV3drs786202350
GWAS Ctlgrs786202350
Max Magnitude0
ClinVar
Risk rs786202350(;)
Alt rs786202350(;)
Reference rs786202350(T;T)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome Ataxia-telangiectasia syndrome
Variation info
Gene ATM
CLNDBN Hereditary cancer-predisposing syndrome Ataxia-telangiectasia syndrome
Reversed 0
HGVS NC_000011.9:g.108158385delT
CLNSRC
CLNACC RCV000165114.1, RCV000205906.1,