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rs587779872

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs587779872(C;T)
Make rs587779872(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome11
Position108345818
GeneATM, C11orf65
is asnp
is mentioned by
dbSNPrs587779872
ebirs587779872
HLIrs587779872
Exacrs587779872
Varsomers587779872
Maprs587779872
PheGenIrs587779872
hapmaprs587779872
1000 genomesrs587779872
hgdprs587779872
ensemblrs587779872
gopubmedrs587779872
geneviewrs587779872
scholarrs587779872
googlers587779872
pharmgkbrs587779872
gwascentralrs587779872
openSNPrs587779872
23andMers587779872
23andMe allrs587779872
SNP Nexus

SNPshotrs587779872
SNPdbers587779872
MSV3drs587779872
GWAS Ctlgrs587779872
Max Magnitude0
ClinVar
Risk rs587779872(T;T)
Alt rs587779872(T;T)
Reference rs587779872(C;C)
Significance Other
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.108216545C>T
CLNSRC
CLNACC RCV000115265.5, RCV000169354.2, RCV000212084.1,