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rs7700790

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in complete genomics
Make rs7700790(G;T)
Make rs7700790(T;T)
ReferenceGRCh38 38.1/141
Chromosome5
Position151366778
is asnp
is mentioned by
dbSNPrs7700790
ebirs7700790
HLIrs7700790
Exacrs7700790
Varsomers7700790
Maprs7700790
PheGenIrs7700790
hapmaprs7700790
1000 genomesrs7700790
hgdprs7700790
ensemblrs7700790
gopubmedrs7700790
geneviewrs7700790
scholarrs7700790
googlers7700790
pharmgkbrs7700790
gwascentralrs7700790
openSNPrs7700790
23andMers7700790
23andMe allrs7700790
SNP Nexus

SNPshotrs7700790
SNPdbers7700790
MSV3drs7700790
GWAS Ctlgrs7700790
GMAF0.1419
Max Magnitude0

[PMID 21093336OA-icon.png] Betaine-homocysteine methyltransferase: human liver genotype-phenotype correlation