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rs730881295

From SNPedia

Orientationplus
Geno Mag Summary
(GTGA;GTGA) 0 common in clinvar
Make rs730881295(-;-)
Make rs730881295(-;GTGA)
ReferenceGRCh38.p2 38.2/144
Chromosome11
Position108343376
GeneATM, C11orf65
is asnp
is mentioned by
dbSNPrs730881295
ebirs730881295
HLIrs730881295
Exacrs730881295
Varsomers730881295
Maprs730881295
PheGenIrs730881295
hapmaprs730881295
1000 genomesrs730881295
hgdprs730881295
ensemblrs730881295
gopubmedrs730881295
geneviewrs730881295
scholarrs730881295
googlers730881295
pharmgkbrs730881295
gwascentralrs730881295
openSNPrs730881295
23andMers730881295
23andMe allrs730881295
SNP Nexus

SNPshotrs730881295
SNPdbers730881295
MSV3drs730881295
GWAS Ctlgrs730881295
Max Magnitude0
ClinVar
Risk rs730881295(;)
Alt rs730881295(;)
Reference rs730881295(GTGA;GTGA)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome Ataxia-telangiectasia syndrome not provided
Variation info
Gene C11orf65 ATM
CLNDBN Hereditary cancer-predisposing syndrome Ataxia-telangiectasia syndrome not provided
Reversed 0
HGVS NC_000011.9:g.108214103_108214106delGTGA
CLNSRC
CLNACC RCV000159624.3, RCV000204238.2, RCV000212083.2,