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rs587779878

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs587779878(-;-)
Make rs587779878(-;C)
ReferenceGRCh38.p2 38.2/144
Chromosome11
Position108365449
GeneATM, C11orf65
is asnp
is mentioned by
dbSNPrs587779878
ebirs587779878
HLIrs587779878
Exacrs587779878
Varsomers587779878
Maprs587779878
PheGenIrs587779878
hapmaprs587779878
1000 genomesrs587779878
hgdprs587779878
ensemblrs587779878
gopubmedrs587779878
geneviewrs587779878
scholarrs587779878
googlers587779878
pharmgkbrs587779878
gwascentralrs587779878
openSNPrs587779878
23andMers587779878
23andMe allrs587779878
SNP Nexus

SNPshotrs587779878
SNPdbers587779878
MSV3drs587779878
GWAS Ctlgrs587779878
Max Magnitude0
ClinVar
Risk rs587779878(;)
Alt rs587779878(;)
Reference rs587779878(C;C)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene C11orf65 ATM
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000011.9:g.108236176delC
CLNSRC
CLNACC RCV000115276.2,