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

rs730881359

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs730881359(A;G)
Make rs730881359(G;G)
ReferenceGRCh38.p2 38.2/144
Chromosome11
Position108227625
GeneATM
is asnp
is mentioned by
dbSNPrs730881359
ebirs730881359
HLIrs730881359
Exacrs730881359
Varsomers730881359
Maprs730881359
PheGenIrs730881359
hapmaprs730881359
1000 genomesrs730881359
hgdprs730881359
ensemblrs730881359
gopubmedrs730881359
geneviewrs730881359
scholarrs730881359
googlers730881359
pharmgkbrs730881359
gwascentralrs730881359
openSNPrs730881359
23andMers730881359
23andMe allrs730881359
SNP Nexus

SNPshotrs730881359
SNPdbers730881359
MSV3drs730881359
GWAS Ctlgrs730881359
Max Magnitude0
ClinVar
Risk rs730881359(C,G;C,G)
Alt rs730881359(C,G;C,G)
Reference rs730881359(A;A)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene ATM
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000011.9:g.108098352A>C; NC_000011.9:g.108098352A>G
CLNSRC
CLNACC RCV000166918.1, RCV000159709.1,