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rs371638537

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs371638537(A;T)
Make rs371638537(T;T)
ReferenceGRCh38 38.1/142
Chromosome11
Position108335959
GeneATM, C11orf65
is asnp
is mentioned by
dbSNPrs371638537
ebirs371638537
HLIrs371638537
Exacrs371638537
Varsomers371638537
Maprs371638537
PheGenIrs371638537
hapmaprs371638537
1000 genomesrs371638537
hgdprs371638537
ensemblrs371638537
gopubmedrs371638537
geneviewrs371638537
scholarrs371638537
googlers371638537
pharmgkbrs371638537
gwascentralrs371638537
openSNPrs371638537
23andMers371638537
23andMe allrs371638537
SNP Nexus

SNPshotrs371638537
SNPdbers371638537
MSV3drs371638537
GWAS Ctlgrs371638537
Max Magnitude0
ClinVar
Risk rs371638537(T;T)
Alt rs371638537(T;T)
Reference rs371638537(A;A)
Significance Other
Disease Tumor susceptibility linked to germline BAP1 mutations Ataxia-telangiectasia syndrome Hereditary cancer-predisposing syndrome not provided
Variation info
Gene C11orf65 ATM
CLNDBN Tumor susceptibility linked to germline BAP1 mutations Ataxia-telangiectasia syndrome Hereditary cancer-predisposing syndrome not provided
Reversed 0
HGVS NC_000011.9:g.108206686A>C; NC_000011.9:g.108206686A>T
CLNSRC Ambry Genetics ClinVar
CLNACC RCV000216787.1, RCV000122886.5, RCV000128904.4, RCV000212082.1,