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

rs786203807

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs786203807(-;-)
Make rs786203807(-;C)
ReferenceGRCh38.p2 38.2/146
Chromosome11
Position108256219
GeneATM
is asnp
is mentioned by
dbSNPrs786203807
ebirs786203807
HLIrs786203807
Exacrs786203807
Varsomers786203807
Maprs786203807
PheGenIrs786203807
hapmaprs786203807
1000 genomesrs786203807
hgdprs786203807
ensemblrs786203807
gopubmedrs786203807
geneviewrs786203807
scholarrs786203807
googlers786203807
pharmgkbrs786203807
gwascentralrs786203807
openSNPrs786203807
23andMers786203807
23andMe allrs786203807
SNP Nexus

SNPshotrs786203807
SNPdbers786203807
MSV3drs786203807
GWAS Ctlgrs786203807
Max Magnitude0
ClinVar
Risk rs786203807(;)
Alt rs786203807(;)
Reference rs786203807(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.108126946delC
CLNSRC
CLNACC RCV000167269.1,