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rs780905851

From SNPedia

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Geno Mag Summary
(T;T) 0 common in clinvar
Make rs780905851(A;A)
Make rs780905851(A;T)
ReferenceGRCh38.p2 38.2/147
Chromosome11
Position108345889
GeneATM, C11orf65
is asnp
is mentioned by
dbSNPrs780905851
ebirs780905851
HLIrs780905851
Exacrs780905851
Varsomers780905851
Maprs780905851
PheGenIrs780905851
hapmaprs780905851
1000 genomesrs780905851
hgdprs780905851
ensemblrs780905851
gopubmedrs780905851
geneviewrs780905851
scholarrs780905851
googlers780905851
pharmgkbrs780905851
gwascentralrs780905851
openSNPrs780905851
23andMers780905851
23andMe allrs780905851
SNP Nexus

SNPshotrs780905851
SNPdbers780905851
MSV3drs780905851
GWAS Ctlgrs780905851
Max Magnitude0
ClinVar
Risk rs780905851(A,C,G;A,C,G)
Alt rs780905851(A,C,G;A,C,G)
Reference rs780905851(T;T)
Significance Probable-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.108216616T>G
CLNSRC
CLNACC RCV000220309.1,