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rs876659010

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs876659010(-;-)
Make rs876659010(-;A)
Make rs876659010(A;A)
ReferenceGRCh38.p2 38.2/147
Chromosome11
Position108345838
GeneATM, C11orf65
is asnp
is mentioned by
dbSNPrs876659010
ebirs876659010
HLIrs876659010
Exacrs876659010
Varsomers876659010
Maprs876659010
PheGenIrs876659010
hapmaprs876659010
1000 genomesrs876659010
hgdprs876659010
ensemblrs876659010
gopubmedrs876659010
geneviewrs876659010
scholarrs876659010
googlers876659010
pharmgkbrs876659010
gwascentralrs876659010
openSNPrs876659010
23andMers876659010
23andMe allrs876659010
SNP Nexus

SNPshotrs876659010
SNPdbers876659010
MSV3drs876659010
GWAS Ctlgrs876659010
Max Magnitude0
ClinVar
Risk rs876659010(A;A)
Alt rs876659010(A;A)
Reference rs876659010(;)
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.108216565dupA
CLNSRC
CLNACC RCV000221706.1,