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rs1064793518

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Chromosome11
Position108246963
GeneATM
is asnp
is mentioned by
dbSNPrs1064793518
dbSNP (old)rs1064793518
ClinGenrs1064793518
ebirs1064793518
HLIrs1064793518
Exacrs1064793518
Gnomadrs1064793518
Varsomers1064793518
Maprs1064793518
PheGenIrs1064793518
Biobankrs1064793518
1000 genomesrs1064793518
hgdprs1064793518
ensemblrs1064793518
gopubmedrs1064793518
geneviewrs1064793518
scholarrs1064793518
googlers1064793518
pharmgkbrs1064793518
gwascentralrs1064793518
openSNPrs1064793518
23andMers1064793518
23andMe allrs1064793518
SNPshotrs1064793518
SNPdbers1064793518
MSV3drs1064793518
GWAS Ctlgrs1064793518
Max Magnitude0
ClinVar
Risk rs1064793518(T;T)
Alt rs1064793518(T;T)
Reference Rs1064793518(G;G)
Significance Pathogenic
Disease not provided Hereditary cancer-predisposing syndrome
Variation info
Gene ATM
CLNDBN not provided Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000011.9:g.108117690G>T
CLNSRC
CLNACC RCV000478968.1, RCV000493667.1,