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rs730881293

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs730881293(-;-)
Make rs730881293(-;GA)
Make rs730881293(GA;GA)
ReferenceGRCh38.p2 38.2/144
Chromosome11
Position108332812
GeneATM, C11orf65
is asnp
is mentioned by
dbSNPrs730881293
ebirs730881293
HLIrs730881293
Exacrs730881293
Varsomers730881293
Maprs730881293
PheGenIrs730881293
hapmaprs730881293
1000 genomesrs730881293
hgdprs730881293
ensemblrs730881293
gopubmedrs730881293
geneviewrs730881293
scholarrs730881293
googlers730881293
pharmgkbrs730881293
gwascentralrs730881293
openSNPrs730881293
23andMers730881293
23andMe allrs730881293
SNP Nexus

SNPshotrs730881293
SNPdbers730881293
MSV3drs730881293
GWAS Ctlgrs730881293
Max Magnitude0
ClinVar
Risk rs730881293(GA;GA)
Alt rs730881293(GA;GA)
Reference rs730881293(;)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene C11orf65 ATM
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000011.9:g.108203538_108203539dupGA
CLNSRC
CLNACC RCV000159622.1,