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rs876660411

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs876660411(-;-)
Make rs876660411(-;A)
Make rs876660411(A;A)
ReferenceGRCh38.p2 38.2/147
Chromosome11
Position108347318
GeneATM, C11orf65
is asnp
is mentioned by
dbSNPrs876660411
ebirs876660411
HLIrs876660411
Exacrs876660411
Varsomers876660411
Maprs876660411
PheGenIrs876660411
hapmaprs876660411
1000 genomesrs876660411
hgdprs876660411
ensemblrs876660411
gopubmedrs876660411
geneviewrs876660411
scholarrs876660411
googlers876660411
pharmgkbrs876660411
gwascentralrs876660411
openSNPrs876660411
23andMers876660411
23andMe allrs876660411
SNP Nexus

SNPshotrs876660411
SNPdbers876660411
MSV3drs876660411
GWAS Ctlgrs876660411
Max Magnitude0
ClinVar
Risk rs876660411(A;A)
Alt rs876660411(A;A)
Reference rs876660411(;)
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.108218045dupA
CLNSRC
CLNACC RCV000223413.1,