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rs3092844

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in complete genomics
Make rs3092844(C;T)
Make rs3092844(T;T)
ReferenceGRCh38 38.1/141
Chromosome11
Position108368580
GeneATM, C11orf65
is asnp
is mentioned by
dbSNPrs3092844
dbSNP (classic)rs3092844
ClinGenrs3092844
ebirs3092844
HLIrs3092844
Exacrs3092844
Gnomadrs3092844
Varsomers3092844
LitVarrs3092844
Maprs3092844
PheGenIrs3092844
Biobankrs3092844
1000 genomesrs3092844
hgdprs3092844
ensemblrs3092844
geneviewrs3092844
scholarrs3092844
googlers3092844
pharmgkbrs3092844
gwascentralrs3092844
openSNPrs3092844
23andMers3092844
SNPshotrs3092844
SNPdbers3092844
MSV3drs3092844
GWAS Ctlgrs3092844
GMAF0.04591
Max Magnitude0
? (C;C) (C;T) (T;T) 28


[PMID 22529920OA-icon.png] Computational Refinement of Functional Single Nucleotide Polymorphisms Associated with ATM Gene


ClinVar
Risk rs3092844(A;A) rs3092844(T;T)
Alt rs3092844(A;A) rs3092844(T;T)
Reference Rs3092844(C;C)
Significance Probable-non-pathogenic
Disease Ataxia-telangiectasia syndrome
Variation info
Gene C11orf65 ATM
CLNDBN Ataxia-telangiectasia syndrome
Reversed 0
HGVS NC_000011.9:g.108239307C>T
CLNSRC
CLNACC RCV000343133.1,