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rs587779844

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs587779844(C;T)
Make rs587779844(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome11
Position108301698
GeneATM
is asnp
is mentioned by
dbSNPrs587779844
ebirs587779844
HLIrs587779844
Exacrs587779844
Varsomers587779844
Maprs587779844
PheGenIrs587779844
hapmaprs587779844
1000 genomesrs587779844
hgdprs587779844
ensemblrs587779844
gopubmedrs587779844
geneviewrs587779844
scholarrs587779844
googlers587779844
pharmgkbrs587779844
gwascentralrs587779844
openSNPrs587779844
23andMers587779844
23andMe allrs587779844
SNP Nexus

SNPshotrs587779844
SNPdbers587779844
MSV3drs587779844
GWAS Ctlgrs587779844
Max Magnitude0
ClinVar
Risk rs587779844(T;T)
Alt rs587779844(T;T)
Reference rs587779844(C;C)
Significance Probable-Pathogenic
Disease not specified Ataxia-telangiectasia syndrome Tumor susceptibility linked to germline BAP1 mutations
Variation info
Gene ATM
CLNDBN not specified Ataxia-telangiectasia syndrome Tumor susceptibility linked to germline BAP1 mutations
Reversed 0
HGVS NC_000011.9:g.108172425C>T
CLNSRC
CLNACC RCV000115208.3, RCV000168297.2, RCV000220146.1,