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rs786203888

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs786203888(C;T)
Make rs786203888(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome11
Position108227854
GeneATM
is asnp
is mentioned by
dbSNPrs786203888
ebirs786203888
HLIrs786203888
Exacrs786203888
Varsomers786203888
Maprs786203888
PheGenIrs786203888
hapmaprs786203888
1000 genomesrs786203888
hgdprs786203888
ensemblrs786203888
gopubmedrs786203888
geneviewrs786203888
scholarrs786203888
googlers786203888
pharmgkbrs786203888
gwascentralrs786203888
openSNPrs786203888
23andMers786203888
23andMe allrs786203888
SNP Nexus

SNPshotrs786203888
SNPdbers786203888
MSV3drs786203888
GWAS Ctlgrs786203888
Max Magnitude0
ClinVar
Risk rs786203888(T;T)
Alt rs786203888(T;T)
Reference rs786203888(C;C)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene ATM
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000011.9:g.108098581C>T
CLNSRC
CLNACC RCV000167389.1,