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rs786202087

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs786202087(A;G)
Make rs786202087(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome11
Position108365323
GeneATM, C11orf65
is asnp
is mentioned by
dbSNPrs786202087
ebirs786202087
HLIrs786202087
Exacrs786202087
Varsomers786202087
Maprs786202087
PheGenIrs786202087
hapmaprs786202087
1000 genomesrs786202087
hgdprs786202087
ensemblrs786202087
gopubmedrs786202087
geneviewrs786202087
scholarrs786202087
googlers786202087
pharmgkbrs786202087
gwascentralrs786202087
openSNPrs786202087
23andMers786202087
23andMe allrs786202087
SNP Nexus

SNPshotrs786202087
SNPdbers786202087
MSV3drs786202087
GWAS Ctlgrs786202087
Max Magnitude0
ClinVar
Risk rs786202087(G;G)
Alt rs786202087(G;G)
Reference rs786202087(A;A)
Significance Probable-Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene C11orf65 ATM
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000011.9:g.108236050A>G
CLNSRC
CLNACC RCV000164726.1,