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rs121434216

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs121434216(G;G)
Make rs121434216(G;T)
ReferenceGRCh38 38.1/141
Chromosome11
Position108345804
GeneATM, C11orf65
is asnp
is mentioned by
dbSNPrs121434216
ebirs121434216
HLIrs121434216
Exacrs121434216
Varsomers121434216
Maprs121434216
PheGenIrs121434216
hapmaprs121434216
1000 genomesrs121434216
hgdprs121434216
ensemblrs121434216
gopubmedrs121434216
geneviewrs121434216
scholarrs121434216
googlers121434216
pharmgkbrs121434216
gwascentralrs121434216
openSNPrs121434216
23andMers121434216
23andMe allrs121434216
SNP Nexus

SNPshotrs121434216
SNPdbers121434216
MSV3drs121434216
GWAS Ctlgrs121434216
Merged fromRs28942101
Max Magnitude0
OMIM607585
Desc
Variant0006
Relatedalso
ClinVar
Risk rs121434216(G;G)
Alt rs121434216(G;G)
Reference rs121434216(T;T)
Significance Pathogenic
Disease Ataxia-telangiectasia variant
Variation info
Gene C11orf65 ATM
CLNDBN Ataxia-telangiectasia variant
Reversed 0
HGVS NC_000011.9:g.108216531T>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000003158.3,