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rs17174393

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs17174393(A;A)
Make rs17174393(A;G)
ReferenceGRCh38 38.1/142
Chromosome11
Position108353881
GeneATM, C11orf65
is asnp
is mentioned by
dbSNPrs17174393
ebirs17174393
HLIrs17174393
Exacrs17174393
Varsomers17174393
Maprs17174393
PheGenIrs17174393
hapmaprs17174393
1000 genomesrs17174393
hgdprs17174393
ensemblrs17174393
gopubmedrs17174393
geneviewrs17174393
scholarrs17174393
googlers17174393
pharmgkbrs17174393
gwascentralrs17174393
openSNPrs17174393
23andMers17174393
23andMe allrs17174393
SNP Nexus

SNPshotrs17174393
SNPdbers17174393
MSV3drs17174393
GWAS Ctlgrs17174393
Max Magnitude0


ClinVar
Risk rs17174393(A,C,T;A,C,T)
Alt rs17174393(A,C,T;A,C,T)
Reference rs17174393(G;G)
Significance Other
Disease not provided Ataxia-telangiectasia syndrome Tumor susceptibility linked to germline BAP1 mutations Hereditary cancer-predisposing syndrome
Variation info
Gene C11orf65 ATM
CLNDBN not provided Ataxia-telangiectasia syndrome Tumor susceptibility linked to germline BAP1 mutations Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000011.9:g.108224608G>A; NC_000011.9:g.108224608G>C; NC_000011.9:g.108224608G>T
CLNSRC ClinVar GeneDx
CLNACC RCV000115269.2, RCV000169303.2, RCV000220586.1, RCV000166748.1, RCV000196816.1, RCV000164050.1,