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rs587780645

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs587780645(-;-)
Make rs587780645(-;A)
Make rs587780645(A;A)
ReferenceGRCh38.p2 38.2/144
Chromosome11
Position108365416
GeneATM, C11orf65
is asnp
is mentioned by
dbSNPrs587780645
ebirs587780645
HLIrs587780645
Exacrs587780645
Varsomers587780645
Maprs587780645
PheGenIrs587780645
hapmaprs587780645
1000 genomesrs587780645
hgdprs587780645
ensemblrs587780645
gopubmedrs587780645
geneviewrs587780645
scholarrs587780645
googlers587780645
pharmgkbrs587780645
gwascentralrs587780645
openSNPrs587780645
23andMers587780645
23andMe allrs587780645
SNP Nexus

SNPshotrs587780645
SNPdbers587780645
MSV3drs587780645
GWAS Ctlgrs587780645
Max Magnitude0
ClinVar
Risk rs587780645(A;A)
Alt rs587780645(A;A)
Reference rs587780645(;)
Significance Pathogenic
Disease Ataxia-telangiectasia syndrome Tumor susceptibility linked to germline BAP1 mutations
Variation info
Gene C11orf65 ATM
CLNDBN Ataxia-telangiectasia syndrome Tumor susceptibility linked to germline BAP1 mutations
Reversed 0
HGVS NC_000011.9:g.108236143dupA
CLNSRC
CLNACC RCV000122895.1, RCV000220797.1,