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rs786203059

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs786203059(C;C)
Make rs786203059(C;T)
ReferenceGRCh38.p2 38.2/146
Chromosome11
Position108331559
GeneATM, C11orf65
is asnp
is mentioned by
dbSNPrs786203059
ebirs786203059
HLIrs786203059
Exacrs786203059
Varsomers786203059
Maprs786203059
PheGenIrs786203059
hapmaprs786203059
1000 genomesrs786203059
hgdprs786203059
ensemblrs786203059
gopubmedrs786203059
geneviewrs786203059
scholarrs786203059
googlers786203059
pharmgkbrs786203059
gwascentralrs786203059
openSNPrs786203059
23andMers786203059
23andMe allrs786203059
SNP Nexus

SNPshotrs786203059
SNPdbers786203059
MSV3drs786203059
GWAS Ctlgrs786203059
Max Magnitude0
ClinVar
Risk rs786203059(C;C)
Alt rs786203059(C;C)
Reference rs786203059(T;T)
Significance Probable-Pathogenic
Disease Hereditary cancer-predisposing syndrome not provided
Variation info
Gene C11orf65 ATM
CLNDBN Hereditary cancer-predisposing syndrome not provided
Reversed 0
HGVS NC_000011.9:g.108202286T>C
CLNSRC
CLNACC RCV000166196.1, RCV000236019.1,