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rs11254385

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs11254385(A;A)
Make rs11254385(A;C)
ReferenceGRCh38.p7 38.3/150
Chromosome10
Position17129763
GeneCUBN
is asnp
is mentioned by
dbSNPrs11254385
dbSNP (old)rs11254385
ClinGenrs11254385
ebirs11254385
HLIrs11254385
Exacrs11254385
Gnomadrs11254385
Varsomers11254385
Maprs11254385
PheGenIrs11254385
Biobankrs11254385
1000 genomesrs11254385
hgdprs11254385
ensemblrs11254385
gopubmedrs11254385
geneviewrs11254385
scholarrs11254385
googlers11254385
pharmgkbrs11254385
gwascentralrs11254385
openSNPrs11254385
23andMers11254385
23andMe allrs11254385
SNPshotrs11254385
SNPdbers11254385
MSV3drs11254385
GWAS Ctlgrs11254385
Max Magnitude0
? (A;A) (A;C) (C;C) 28
ClinVar
Risk rs11254385(A;A)
Alt rs11254385(A;A)
Reference Rs11254385(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene CUBN
CLNDBN not provided
Reversed 0
HGVS NC_000010.10:g.17171762C>A
CLNSRC
CLNACC RCV000413849.1,