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rs876660038

From SNPedia

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Geno Mag Summary
(G;G) 0 common in clinvar
Make rs876660038(A;A)
Make rs876660038(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome11
Position108248932
GeneATM
is asnp
is mentioned by
dbSNPrs876660038
ebirs876660038
HLIrs876660038
Exacrs876660038
Varsomers876660038
Maprs876660038
PheGenIrs876660038
hapmaprs876660038
1000 genomesrs876660038
hgdprs876660038
ensemblrs876660038
gopubmedrs876660038
geneviewrs876660038
scholarrs876660038
googlers876660038
pharmgkbrs876660038
gwascentralrs876660038
openSNPrs876660038
23andMers876660038
23andMe allrs876660038
SNP Nexus

SNPshotrs876660038
SNPdbers876660038
MSV3drs876660038
GWAS Ctlgrs876660038
Max Magnitude0
ClinVar
Risk rs876660038(A;A)
Alt rs876660038(A;A)
Reference rs876660038(G;G)
Significance Probable-Pathogenic
Disease Tumor susceptibility linked to germline BAP1 mutations
Variation info
Gene ATM
CLNDBN Tumor susceptibility linked to germline BAP1 mutations
Reversed 0
HGVS NC_000011.9:g.108119659G>A
CLNSRC
CLNACC RCV000223052.1,