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rs17007417

From SNPedia

Orientationplus
Stabilizedplus
Make rs17007417(C;C)
Make rs17007417(C;T)
Make rs17007417(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome2
Position71808541
is asnp
is mentioned by
dbSNPrs17007417
dbSNP (classic)rs17007417
ClinGenrs17007417
ebirs17007417
HLIrs17007417
Exacrs17007417
Gnomadrs17007417
Varsomers17007417
LitVarrs17007417
Maprs17007417
PheGenIrs17007417
Biobankrs17007417
1000 genomesrs17007417
hgdprs17007417
ensemblrs17007417
geneviewrs17007417
scholarrs17007417
googlers17007417
pharmgkbrs17007417
gwascentralrs17007417
openSNPrs17007417
23andMers17007417
23andMe allrs17007417
SNPshotrs17007417
SNPdbers17007417
MSV3drs17007417
GWAS Ctlgrs17007417
Max Magnitude0
? (C;C) (C;T) (T;T) 28


[PMID 29385134OA-icon.png] Risk estimation model for nonalcoholic fatty liver disease in the Japanese using multiple genetic markers.