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

rs786203817

From SNPedia

Orientationplus
Geno Mag Summary
(TT;TT) 0 common in clinvar
Make rs786203817(-;-)
Make rs786203817(-;TT)
ReferenceGRCh38.p2 38.2/146
Chromosome11
Position108282759
GeneATM
is asnp
is mentioned by
dbSNPrs786203817
ebirs786203817
HLIrs786203817
Exacrs786203817
Varsomers786203817
Maprs786203817
PheGenIrs786203817
hapmaprs786203817
1000 genomesrs786203817
hgdprs786203817
ensemblrs786203817
gopubmedrs786203817
geneviewrs786203817
scholarrs786203817
googlers786203817
pharmgkbrs786203817
gwascentralrs786203817
openSNPrs786203817
23andMers786203817
23andMe allrs786203817
SNP Nexus

SNPshotrs786203817
SNPdbers786203817
MSV3drs786203817
GWAS Ctlgrs786203817
Max Magnitude0
ClinVar
Risk rs786203817(;)
Alt rs786203817(;)
Reference rs786203817(TT;TT)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome not provided
Variation info
Gene ATM
CLNDBN Hereditary cancer-predisposing syndrome not provided
Reversed 0
HGVS NC_000011.9:g.108153486_108153487delTT
CLNSRC
CLNACC RCV000167290.1, RCV000235460.1,