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rs730881364

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs730881364(C;C)
Make rs730881364(C;G)
ReferenceGRCh38.p2 38.2/144
Chromosome11
Position108284226
GeneATM
is asnp
is mentioned by
dbSNPrs730881364
ebirs730881364
HLIrs730881364
Exacrs730881364
Varsomers730881364
Maprs730881364
PheGenIrs730881364
hapmaprs730881364
1000 genomesrs730881364
hgdprs730881364
ensemblrs730881364
gopubmedrs730881364
geneviewrs730881364
scholarrs730881364
googlers730881364
pharmgkbrs730881364
gwascentralrs730881364
openSNPrs730881364
23andMers730881364
23andMe allrs730881364
SNP Nexus

SNPshotrs730881364
SNPdbers730881364
MSV3drs730881364
GWAS Ctlgrs730881364
Max Magnitude0
ClinVar
Risk rs730881364(C;C)
Alt rs730881364(C;C)
Reference rs730881364(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene ATM
CLNDBN not provided
Reversed 0
HGVS NC_000011.9:g.108154953G>C
CLNSRC
CLNACC RCV000159717.1,