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

rs730881333

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs730881333(C;T)
Make rs730881333(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome11
Position108243994
GeneATM
is asnp
is mentioned by
dbSNPrs730881333
ebirs730881333
HLIrs730881333
Exacrs730881333
Varsomers730881333
Maprs730881333
PheGenIrs730881333
hapmaprs730881333
1000 genomesrs730881333
hgdprs730881333
ensemblrs730881333
gopubmedrs730881333
geneviewrs730881333
scholarrs730881333
googlers730881333
pharmgkbrs730881333
gwascentralrs730881333
openSNPrs730881333
23andMers730881333
23andMe allrs730881333
SNP Nexus

SNPshotrs730881333
SNPdbers730881333
MSV3drs730881333
GWAS Ctlgrs730881333
Max Magnitude0
ClinVar
Risk rs730881333(A,T;A,T)
Alt rs730881333(A,T;A,T)
Reference rs730881333(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene ATM
CLNDBN not provided
Reversed 0
HGVS NC_000011.9:g.108114721C>T
CLNSRC
CLNACC RCV000159674.1,