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rs770641163

From SNPedia

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Geno Mag Summary
(C;C) 0 common in clinvar
Make rs770641163(C;T)
Make rs770641163(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome11
Position108365208
GeneATM, C11orf65
is asnp
is mentioned by
dbSNPrs770641163
ebirs770641163
HLIrs770641163
Exacrs770641163
Varsomers770641163
Maprs770641163
PheGenIrs770641163
hapmaprs770641163
1000 genomesrs770641163
hgdprs770641163
ensemblrs770641163
gopubmedrs770641163
geneviewrs770641163
scholarrs770641163
googlers770641163
pharmgkbrs770641163
gwascentralrs770641163
openSNPrs770641163
23andMers770641163
23andMe allrs770641163
SNP Nexus

SNPshotrs770641163
SNPdbers770641163
MSV3drs770641163
GWAS Ctlgrs770641163
Max Magnitude0
ClinVar
Risk rs770641163(T;T)
Alt rs770641163(T;T)
Reference rs770641163(C;C)
Significance Other
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.108235935C>T
CLNSRC Western University
CLNACC RCV000165909.1, RCV000169469.2,