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rs786203489

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs786203489(-;-)
Make rs786203489(-;A)
ReferenceGRCh38.p2 38.2/146
Chromosome11
Position108365173
GeneATM, C11orf65
is asnp
is mentioned by
dbSNPrs786203489
ebirs786203489
HLIrs786203489
Exacrs786203489
Varsomers786203489
Maprs786203489
PheGenIrs786203489
hapmaprs786203489
1000 genomesrs786203489
hgdprs786203489
ensemblrs786203489
gopubmedrs786203489
geneviewrs786203489
scholarrs786203489
googlers786203489
pharmgkbrs786203489
gwascentralrs786203489
openSNPrs786203489
23andMers786203489
23andMe allrs786203489
SNP Nexus

SNPshotrs786203489
SNPdbers786203489
MSV3drs786203489
GWAS Ctlgrs786203489
Max Magnitude0
ClinVar
Risk rs786203489(;)
Alt rs786203489(;)
Reference rs786203489(A;A)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene C11orf65 ATM
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000011.9:g.108235900delA
CLNSRC
CLNACC RCV000166811.1,