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rs730881362

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs730881362(G;T)
Make rs730881362(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome11
Position108227857
GeneATM
is asnp
is mentioned by
dbSNPrs730881362
ebirs730881362
HLIrs730881362
Exacrs730881362
Varsomers730881362
Maprs730881362
PheGenIrs730881362
hapmaprs730881362
1000 genomesrs730881362
hgdprs730881362
ensemblrs730881362
gopubmedrs730881362
geneviewrs730881362
scholarrs730881362
googlers730881362
pharmgkbrs730881362
gwascentralrs730881362
openSNPrs730881362
23andMers730881362
23andMe allrs730881362
SNP Nexus

SNPshotrs730881362
SNPdbers730881362
MSV3drs730881362
GWAS Ctlgrs730881362
Max Magnitude0
ClinVar
Risk rs730881362(T;T)
Alt rs730881362(T;T)
Reference rs730881362(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene ATM
CLNDBN not provided
Reversed 0
HGVS NC_000011.9:g.108098584G>T
CLNSRC
CLNACC RCV000159713.2,