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rs730881388

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs730881388(C;T)
Make rs730881388(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome11
Position108271378
GeneATM
is asnp
is mentioned by
dbSNPrs730881388
ebirs730881388
HLIrs730881388
Exacrs730881388
Varsomers730881388
Maprs730881388
PheGenIrs730881388
hapmaprs730881388
1000 genomesrs730881388
hgdprs730881388
ensemblrs730881388
gopubmedrs730881388
geneviewrs730881388
scholarrs730881388
googlers730881388
pharmgkbrs730881388
gwascentralrs730881388
openSNPrs730881388
23andMers730881388
23andMe allrs730881388
SNP Nexus

SNPshotrs730881388
SNPdbers730881388
MSV3drs730881388
GWAS Ctlgrs730881388
Max Magnitude0
ClinVar
Risk rs730881388(T;T)
Alt rs730881388(T;T)
Reference rs730881388(C;C)
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.108142105C>T
CLNSRC
CLNACC RCV000159761.3, RCV000211992.1,