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rs1060501695

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1060501695(C;G)
Make rs1060501695(G;G)
ReferenceGRCh38.p7 38.3/150
Chromosome11
Position108335098
GeneATM, C11orf65
is asnp
is mentioned by
dbSNPrs1060501695
dbSNP (classic)rs1060501695
ClinGenrs1060501695
ebirs1060501695
HLIrs1060501695
Exacrs1060501695
Gnomadrs1060501695
Varsomers1060501695
LitVarrs1060501695
Maprs1060501695
PheGenIrs1060501695
Biobankrs1060501695
1000 genomesrs1060501695
hgdprs1060501695
ensemblrs1060501695
geneviewrs1060501695
scholarrs1060501695
googlers1060501695
pharmgkbrs1060501695
gwascentralrs1060501695
openSNPrs1060501695
23andMers1060501695
SNPshotrs1060501695
SNPdbers1060501695
MSV3drs1060501695
GWAS Ctlgrs1060501695
Max Magnitude0
ClinVar
Risk rs1060501695(G;G) rs1060501695(T;T)
Alt rs1060501695(G;G) rs1060501695(T;T)
Reference Rs1060501695(C;C)
Significance Pathogenic
Disease Ataxia-telangiectasia syndrome not provided
Variation info
Gene C11orf65 ATM
CLNDBN Ataxia-telangiectasia syndrome not provided
Reversed 0
HGVS NC_000011.9:g.108205825C>G; NC_000011.9:g.108205825C>T
CLNSRC
CLNACC RCV000471423.1, RCV000480590.1,