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rs1064795885

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Chromosome11
Position108282764
GeneATM
is asnp
is mentioned by
dbSNPrs1064795885
dbSNP (old)rs1064795885
ClinGenrs1064795885
ebirs1064795885
HLIrs1064795885
Exacrs1064795885
Gnomadrs1064795885
Varsomers1064795885
Maprs1064795885
PheGenIrs1064795885
Biobankrs1064795885
1000 genomesrs1064795885
hgdprs1064795885
ensemblrs1064795885
gopubmedrs1064795885
geneviewrs1064795885
scholarrs1064795885
googlers1064795885
pharmgkbrs1064795885
gwascentralrs1064795885
openSNPrs1064795885
23andMers1064795885
23andMe allrs1064795885
SNPshotrs1064795885
SNPdbers1064795885
MSV3drs1064795885
GWAS Ctlgrs1064795885
Max Magnitude0
ClinVar
Risk rs1064795885(-;-)
Alt rs1064795885(-;-)
Reference Rs1064795885(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene ATM
CLNDBN not provided
Reversed 0
HGVS NC_000011.9:g.108153491delG
CLNSRC
CLNACC RCV000485936.1,