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rs641738

From SNPedia

Orientationplus
Make rs641738(C;C)
Make rs641738(C;T)
Make rs641738(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome19
GeneMBOAT7, TMC4
is asnp
is mentioned by
dbSNPrs641738
ebirs641738
HLIrs641738
Exacrs641738
Varsomers641738
Maprs641738
PheGenIrs641738
hapmaprs641738
1000 genomesrs641738
hgdprs641738
ensemblrs641738
gopubmedrs641738
geneviewrs641738
scholarrs641738
googlers641738
pharmgkbrs641738
gwascentralrs641738
openSNPrs641738
23andMers641738
23andMe allrs641738
SNP Nexus

SNPshotrs641738
SNPdbers641738
MSV3drs641738
GWAS Ctlgrs641738
Max Magnitude
? (C;C) (C;T) (T;T) 28

[PMID 26850495] The MBOAT7-TMC4 Variant rs641738 Increases Risk of Nonalcoholic Fatty Liver Disease in Individuals of European Descent.