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rs730881384

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs730881384(A;A)
Make rs730881384(A;C)
ReferenceGRCh38.p2 38.2/144
Chromosome11
Position108333955
GeneATM, C11orf65
is asnp
is mentioned by
dbSNPrs730881384
ebirs730881384
HLIrs730881384
Exacrs730881384
Varsomers730881384
Maprs730881384
PheGenIrs730881384
hapmaprs730881384
1000 genomesrs730881384
hgdprs730881384
ensemblrs730881384
gopubmedrs730881384
geneviewrs730881384
scholarrs730881384
googlers730881384
pharmgkbrs730881384
gwascentralrs730881384
openSNPrs730881384
23andMers730881384
23andMe allrs730881384
SNP Nexus

SNPshotrs730881384
SNPdbers730881384
MSV3drs730881384
GWAS Ctlgrs730881384
Max Magnitude0
ClinVar
Risk rs730881384(A;A)
Alt rs730881384(A;A)
Reference rs730881384(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene C11orf65 ATM
CLNDBN not provided
Reversed 0
HGVS NC_000011.9:g.108204682C>A
CLNSRC
CLNACC RCV000159752.2,