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rs730881303

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs730881303(-;-)
Make rs730881303(-;A)
ReferenceGRCh38.p2 38.2/144
Chromosome11
Position108229229
GeneATM
is asnp
is mentioned by
dbSNPrs730881303
ebirs730881303
HLIrs730881303
Exacrs730881303
Varsomers730881303
Maprs730881303
PheGenIrs730881303
hapmaprs730881303
1000 genomesrs730881303
hgdprs730881303
ensemblrs730881303
gopubmedrs730881303
geneviewrs730881303
scholarrs730881303
googlers730881303
pharmgkbrs730881303
gwascentralrs730881303
openSNPrs730881303
23andMers730881303
23andMe allrs730881303
SNP Nexus

SNPshotrs730881303
SNPdbers730881303
MSV3drs730881303
GWAS Ctlgrs730881303
Max Magnitude0
ClinVar
Risk rs730881303(;)
Alt rs730881303(;)
Reference rs730881303(A;A)
Significance Pathogenic
Disease not provided
Variation info
Gene ATM
CLNDBN not provided
Reversed 0
HGVS NC_000011.9:g.108099956delA
CLNSRC
CLNACC RCV000159632.2,