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rs876660022

From SNPedia

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Geno Mag Summary
(AG;AG) 0 common in clinvar
Make rs876660022(-;-)
Make rs876660022(-;AG)
ReferenceGRCh38.p2 38.2/147
Chromosome11
Position108365338
GeneATM, C11orf65
is asnp
is mentioned by
dbSNPrs876660022
ebirs876660022
HLIrs876660022
Exacrs876660022
Varsomers876660022
Maprs876660022
PheGenIrs876660022
hapmaprs876660022
1000 genomesrs876660022
hgdprs876660022
ensemblrs876660022
gopubmedrs876660022
geneviewrs876660022
scholarrs876660022
googlers876660022
pharmgkbrs876660022
gwascentralrs876660022
openSNPrs876660022
23andMers876660022
23andMe allrs876660022
SNP Nexus

SNPshotrs876660022
SNPdbers876660022
MSV3drs876660022
GWAS Ctlgrs876660022
Max Magnitude0
ClinVar
Risk rs876660022(;)
Alt rs876660022(;)
Reference rs876660022(AG;AG)
Significance Pathogenic
Disease Tumor susceptibility linked to germline BAP1 mutations
Variation info
Gene C11orf65 ATM
CLNDBN Tumor susceptibility linked to germline BAP1 mutations
Reversed 0
HGVS NC_000011.9:g.108236065_108236066delAG
CLNSRC
CLNACC RCV000222939.1,