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rs786202814

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs786202814(-;-)
Make rs786202814(-;C)
ReferenceGRCh38.p2 38.2/146
Chromosome11
Position108310162
GeneATM
is asnp
is mentioned by
dbSNPrs786202814
ebirs786202814
HLIrs786202814
Exacrs786202814
Varsomers786202814
Maprs786202814
PheGenIrs786202814
hapmaprs786202814
1000 genomesrs786202814
hgdprs786202814
ensemblrs786202814
gopubmedrs786202814
geneviewrs786202814
scholarrs786202814
googlers786202814
pharmgkbrs786202814
gwascentralrs786202814
openSNPrs786202814
23andMers786202814
23andMe allrs786202814
SNP Nexus

SNPshotrs786202814
SNPdbers786202814
MSV3drs786202814
GWAS Ctlgrs786202814
Max Magnitude0
ClinVar
Risk rs786202814(;)
Alt rs786202814(;)
Reference rs786202814(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.108180889delC
CLNSRC
CLNACC RCV000165828.1,