Have questions? Visit https://www.reddit.com/r/SNPedia

rs730881297

From SNPedia

Orientationplus
Geno Mag Summary
(AT;AT) 0 common in clinvar
Make rs730881297(-;-)
Make rs730881297(-;TA)
Make rs730881297(TA;TA)
ReferenceGRCh38.p2 38.2/144
Chromosome11
Position108244005
GeneATM
is asnp
is mentioned by
dbSNPrs730881297
ebirs730881297
HLIrs730881297
Exacrs730881297
Varsomers730881297
Maprs730881297
PheGenIrs730881297
hapmaprs730881297
1000 genomesrs730881297
hgdprs730881297
ensemblrs730881297
gopubmedrs730881297
geneviewrs730881297
scholarrs730881297
googlers730881297
pharmgkbrs730881297
gwascentralrs730881297
openSNPrs730881297
23andMers730881297
23andMe allrs730881297
SNP Nexus

SNPshotrs730881297
SNPdbers730881297
MSV3drs730881297
GWAS Ctlgrs730881297
Max Magnitude0
ClinVar
Risk rs730881297(;)
Alt rs730881297(;)
Reference rs730881297(AT;AT)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene ATM
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000011.9:g.108114732_108114733delTA
CLNSRC
CLNACC RCV000159626.1,