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rs876660674

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs876660674(G;T)
Make rs876660674(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome11
Position108289104
GeneATM
is asnp
is mentioned by
dbSNPrs876660674
ebirs876660674
HLIrs876660674
Exacrs876660674
Varsomers876660674
Maprs876660674
PheGenIrs876660674
hapmaprs876660674
1000 genomesrs876660674
hgdprs876660674
ensemblrs876660674
gopubmedrs876660674
geneviewrs876660674
scholarrs876660674
googlers876660674
pharmgkbrs876660674
gwascentralrs876660674
openSNPrs876660674
23andMers876660674
23andMe allrs876660674
SNP Nexus

SNPshotrs876660674
SNPdbers876660674
MSV3drs876660674
GWAS Ctlgrs876660674
Max Magnitude0
ClinVar
Risk rs876660674(T;T)
Alt rs876660674(T;T)
Reference rs876660674(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.108159831G>T
CLNSRC
CLNACC RCV000220335.1,