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rs786204737

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs786204737(-;-)
Make rs786204737(-;T)
ReferenceGRCh38.p2 38.2/146
Chromosome11
Position108250989
GeneATM
is asnp
is mentioned by
dbSNPrs786204737
ebirs786204737
HLIrs786204737
Exacrs786204737
Varsomers786204737
Maprs786204737
PheGenIrs786204737
hapmaprs786204737
1000 genomesrs786204737
hgdprs786204737
ensemblrs786204737
gopubmedrs786204737
geneviewrs786204737
scholarrs786204737
googlers786204737
pharmgkbrs786204737
gwascentralrs786204737
openSNPrs786204737
23andMers786204737
23andMe allrs786204737
SNP Nexus

SNPshotrs786204737
SNPdbers786204737
MSV3drs786204737
GWAS Ctlgrs786204737
Max Magnitude0
ClinVar
Risk rs786204737(;)
Alt rs786204737(;)
Reference rs786204737(T;T)
Significance Probable-Pathogenic
Disease Ataxia-telangiectasia syndrome not provided
Variation info
Gene ATM
CLNDBN Ataxia-telangiectasia syndrome not provided
Reversed 0
HGVS NC_000011.9:g.108121716delT
CLNSRC
CLNACC RCV000169584.1, RCV000236634.1,