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rs1018140779

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
ReferenceGRCh38.p7 38.3/150
Chromosome11
Position108329097
GeneATM, C11orf65
is asnp
is mentioned by
dbSNPrs1018140779
dbSNP (old)rs1018140779
ClinGenrs1018140779
ebirs1018140779
HLIrs1018140779
Exacrs1018140779
Gnomadrs1018140779
Varsomers1018140779
LitVarrs1018140779
Maprs1018140779
PheGenIrs1018140779
Biobankrs1018140779
1000 genomesrs1018140779
hgdprs1018140779
ensemblrs1018140779
gopubmedrs1018140779
geneviewrs1018140779
scholarrs1018140779
googlers1018140779
pharmgkbrs1018140779
gwascentralrs1018140779
openSNPrs1018140779
23andMers1018140779
23andMe allrs1018140779
SNPshotrs1018140779
SNPdbers1018140779
MSV3drs1018140779
GWAS Ctlgrs1018140779
Max Magnitude0
ClinVar
Risk rs1018140779(T;T)
Alt rs1018140779(T;T)
Reference Rs1018140779(C;C)
Significance Probable-Pathogenic
Disease Ataxia-telangiectasia syndrome not specified
Variation info
Gene
CLNDBN Ataxia-telangiectasia syndrome not specified
Reversed 0
HGVS NC_000011.9:g.108199824C>G; NC_000011.9:g.108199824C>T
CLNSRC
CLNACC RCV000411247.1, RCV000436625.1,