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rs876660235

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs876660235(-;-)
Make rs876660235(-;A)
Make rs876660235(A;A)
ReferenceGRCh38.p2 38.2/147
Chromosome11
Position108365358
GeneATM, C11orf65
is asnp
is mentioned by
dbSNPrs876660235
ebirs876660235
HLIrs876660235
Exacrs876660235
Varsomers876660235
Maprs876660235
PheGenIrs876660235
hapmaprs876660235
1000 genomesrs876660235
hgdprs876660235
ensemblrs876660235
gopubmedrs876660235
geneviewrs876660235
scholarrs876660235
googlers876660235
pharmgkbrs876660235
gwascentralrs876660235
openSNPrs876660235
23andMers876660235
23andMe allrs876660235
SNP Nexus

SNPshotrs876660235
SNPdbers876660235
MSV3drs876660235
GWAS Ctlgrs876660235
Max Magnitude0
ClinVar
Risk rs876660235(A;A)
Alt rs876660235(A;A)
Reference rs876660235(;)
Significance Pathogenic
Disease Tumor susceptibility linked to germline BAP1 mutations not provided
Variation info
Gene C11orf65 ATM
CLNDBN Tumor susceptibility linked to germline BAP1 mutations not provided
Reversed 0
HGVS NC_000011.9:g.108236085dupA
CLNSRC
CLNACC RCV000220949.1, RCV000237011.1,