Have questions? Visit https://www.reddit.com/r/SNPedia

rs786203309

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs786203309(G;G)
Make rs786203309(G;T)
ReferenceGRCh38.p2 38.2/146
Chromosome11
Position108268560
GeneATM
is asnp
is mentioned by
dbSNPrs786203309
ebirs786203309
HLIrs786203309
Exacrs786203309
Varsomers786203309
Maprs786203309
PheGenIrs786203309
hapmaprs786203309
1000 genomesrs786203309
hgdprs786203309
ensemblrs786203309
gopubmedrs786203309
geneviewrs786203309
scholarrs786203309
googlers786203309
pharmgkbrs786203309
gwascentralrs786203309
openSNPrs786203309
23andMers786203309
23andMe allrs786203309
SNP Nexus

SNPshotrs786203309
SNPdbers786203309
MSV3drs786203309
GWAS Ctlgrs786203309
Max Magnitude0
ClinVar
Risk rs786203309(G;G)
Alt rs786203309(G;G)
Reference rs786203309(T;T)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene ATM
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000011.9:g.108139287T>G
CLNSRC
CLNACC RCV000166556.1,