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rs786204437

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs786204437(-;-)
Make rs786204437(-;G)
ReferenceGRCh38.p2 38.2/146
Chromosome11
Position108332905
GeneATM, C11orf65
is asnp
is mentioned by
dbSNPrs786204437
ebirs786204437
HLIrs786204437
Exacrs786204437
Varsomers786204437
Maprs786204437
PheGenIrs786204437
hapmaprs786204437
1000 genomesrs786204437
hgdprs786204437
ensemblrs786204437
gopubmedrs786204437
geneviewrs786204437
scholarrs786204437
googlers786204437
pharmgkbrs786204437
gwascentralrs786204437
openSNPrs786204437
23andMers786204437
23andMe allrs786204437
SNP Nexus

SNPshotrs786204437
SNPdbers786204437
MSV3drs786204437
GWAS Ctlgrs786204437
Max Magnitude0
ClinVar
Risk rs786204437(;)
Alt rs786204437(;)
Reference rs786204437(G;G)
Significance Probable-Pathogenic
Disease Ataxia-telangiectasia syndrome
Variation info
Gene C11orf65 ATM
CLNDBN Ataxia-telangiectasia syndrome
Reversed 0
HGVS NC_000011.9:g.108203632delG
CLNSRC
CLNACC RCV000169058.1,