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rs2608555

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs2608555(C;T)
Make rs2608555(T;T)
ReferenceGRCh38 38.1/141
Chromosome16
Position81365030
GeneGAN
is asnp
is mentioned by
dbSNPrs2608555
ebirs2608555
HLIrs2608555
Exacrs2608555
Varsomers2608555
Maprs2608555
PheGenIrs2608555
hapmaprs2608555
1000 genomesrs2608555
hgdprs2608555
ensemblrs2608555
gopubmedrs2608555
geneviewrs2608555
scholarrs2608555
googlers2608555
pharmgkbrs2608555
gwascentralrs2608555
openSNPrs2608555
23andMers2608555
23andMe allrs2608555
SNP Nexus

SNPshotrs2608555
SNPdbers2608555
MSV3drs2608555
GWAS Ctlgrs2608555
GMAF0.157
Max Magnitude0
? (C;C) (C;T) (T;T) 28

[PMID 21859556] Association Study of Selected Genetic Polymorphisms and Occurrence of Venous Thromboembolism in Patients With Multiple Myeloma Who Were Treated With Thalidomide


[PMID 21671989OA-icon.png] Dosing equation for tacrolimus using genetic variants and clinical factors.


ClinVar
Risk rs2608555(T;T)
Alt rs2608555(T;T)
Reference rs2608555(C;C)
Significance Probable-non-pathogenic
Disease not specified
Variation info
Gene GAN
CLNDBN not specified
Reversed 0
HGVS NC_000016.9:g.81398635C>T
CLNSRC ClinVar University of Chicago
CLNACC RCV000117118.2,