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rs730881305

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs730881305(-;-)
Make rs730881305(-;AT)
Make rs730881305(AT;AT)
ReferenceGRCh38.p2 38.2/144
Chromosome11
Position108301671
GeneATM
is asnp
is mentioned by
dbSNPrs730881305
ebirs730881305
HLIrs730881305
Exacrs730881305
Varsomers730881305
Maprs730881305
PheGenIrs730881305
hapmaprs730881305
1000 genomesrs730881305
hgdprs730881305
ensemblrs730881305
gopubmedrs730881305
geneviewrs730881305
scholarrs730881305
googlers730881305
pharmgkbrs730881305
gwascentralrs730881305
openSNPrs730881305
23andMers730881305
23andMe allrs730881305
SNP Nexus

SNPshotrs730881305
SNPdbers730881305
MSV3drs730881305
GWAS Ctlgrs730881305
Max Magnitude0
ClinVar
Risk rs730881305(TA;TA)
Alt rs730881305(TA;TA)
Reference rs730881305(;)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene ATM
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000011.9:g.108172398_108172399insAT
CLNSRC
CLNACC RCV000159634.1,