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rs786202743

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs786202743(C;T)
Make rs786202743(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome11
Position108254013
GeneATM
is asnp
is mentioned by
dbSNPrs786202743
ebirs786202743
HLIrs786202743
Exacrs786202743
Varsomers786202743
Maprs786202743
PheGenIrs786202743
hapmaprs786202743
1000 genomesrs786202743
hgdprs786202743
ensemblrs786202743
gopubmedrs786202743
geneviewrs786202743
scholarrs786202743
googlers786202743
pharmgkbrs786202743
gwascentralrs786202743
openSNPrs786202743
23andMers786202743
23andMe allrs786202743
SNP Nexus

SNPshotrs786202743
SNPdbers786202743
MSV3drs786202743
GWAS Ctlgrs786202743
Max Magnitude0
ClinVar
Risk rs786202743(T;T)
Alt rs786202743(T;T)
Reference rs786202743(C;C)
Significance Other
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene ATM
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000011.9:g.108124740C>T
CLNSRC
CLNACC RCV000165710.2,