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rs786202016

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs786202016(A;A)
Make rs786202016(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome11
Position108312499
GeneATM
is asnp
is mentioned by
dbSNPrs786202016
ebirs786202016
HLIrs786202016
Exacrs786202016
Varsomers786202016
Maprs786202016
PheGenIrs786202016
hapmaprs786202016
1000 genomesrs786202016
hgdprs786202016
ensemblrs786202016
gopubmedrs786202016
geneviewrs786202016
scholarrs786202016
googlers786202016
pharmgkbrs786202016
gwascentralrs786202016
openSNPrs786202016
23andMers786202016
23andMe allrs786202016
SNP Nexus

SNPshotrs786202016
SNPdbers786202016
MSV3drs786202016
GWAS Ctlgrs786202016
Max Magnitude0
ClinVar
Risk rs786202016(A;A)
Alt rs786202016(A;A)
Reference rs786202016(G;G)
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.108183226G>A
CLNSRC
CLNACC RCV000164608.1,