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rs730881302

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs730881302(-;-)
Make rs730881302(-;C)
ReferenceGRCh38.p2 38.2/144
Chromosome11
Position108281118
GeneATM
is asnp
is mentioned by
dbSNPrs730881302
ebirs730881302
HLIrs730881302
Exacrs730881302
Varsomers730881302
Maprs730881302
PheGenIrs730881302
hapmaprs730881302
1000 genomesrs730881302
hgdprs730881302
ensemblrs730881302
gopubmedrs730881302
geneviewrs730881302
scholarrs730881302
googlers730881302
pharmgkbrs730881302
gwascentralrs730881302
openSNPrs730881302
23andMers730881302
23andMe allrs730881302
SNP Nexus

SNPshotrs730881302
SNPdbers730881302
MSV3drs730881302
GWAS Ctlgrs730881302
Max Magnitude0
ClinVar
Risk rs730881302(;)
Alt rs730881302(;)
Reference rs730881302(C;C)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene ATM
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000011.9:g.108151845delC
CLNSRC
CLNACC RCV000159631.1,