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rs786202826

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs786202826(A;G)
Make rs786202826(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome11
Position108353805
GeneATM, C11orf65
is asnp
is mentioned by
dbSNPrs786202826
ebirs786202826
HLIrs786202826
Exacrs786202826
Varsomers786202826
Maprs786202826
PheGenIrs786202826
hapmaprs786202826
1000 genomesrs786202826
hgdprs786202826
ensemblrs786202826
gopubmedrs786202826
geneviewrs786202826
scholarrs786202826
googlers786202826
pharmgkbrs786202826
gwascentralrs786202826
openSNPrs786202826
23andMers786202826
23andMe allrs786202826
SNP Nexus

SNPshotrs786202826
SNPdbers786202826
MSV3drs786202826
GWAS Ctlgrs786202826
Max Magnitude0
ClinVar
Risk rs786202826(G;G)
Alt rs786202826(G;G)
Reference rs786202826(A;A)
Significance Probable-Pathogenic
Disease Hereditary cancer-predisposing syndrome Ataxia-telangiectasia syndrome
Variation info
Gene C11orf65 ATM
CLNDBN Hereditary cancer-predisposing syndrome Ataxia-telangiectasia syndrome
Reversed 0
HGVS NC_000011.9:g.108224532A>G
CLNSRC
CLNACC RCV000165842.1, RCV000230822.1,