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rs587779861

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs587779861(C;T)
Make rs587779861(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome11
Position108329112
GeneATM, C11orf65
is asnp
is mentioned by
dbSNPrs587779861
dbSNP (old)rs587779861
ClinGenrs587779861
ebirs587779861
HLIrs587779861
Exacrs587779861
Gnomadrs587779861
Varsomers587779861
Maprs587779861
PheGenIrs587779861
Biobankrs587779861
1000 genomesrs587779861
hgdprs587779861
ensemblrs587779861
gopubmedrs587779861
geneviewrs587779861
scholarrs587779861
googlers587779861
pharmgkbrs587779861
gwascentralrs587779861
openSNPrs587779861
23andMers587779861
23andMe allrs587779861
SNP Nexus

SNPshotrs587779861
SNPdbers587779861
MSV3drs587779861
GWAS Ctlgrs587779861
Max Magnitude0
ClinVar
Risk rs587779861(T;T)
Alt rs587779861(T;T)
Reference Rs587779861(C;C)
Significance Probable-Pathogenic
Disease not provided Hereditary cancer-predisposing syndrome
Variation info
Gene C11orf65 ATM
CLNDBN not provided Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000011.9:g.108199839C>T
CLNSRC
CLNACC RCV000115242.4, RCV000494662.1,