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rs6022662

From SNPedia

Orientationplus
Stabilizedplus
Make rs6022662(C;C)
Make rs6022662(C;T)
Make rs6022662(T;T)
ReferenceGRCh38 38.1/141
Chromosome20
Position53688088
is asnp
is mentioned by
dbSNPrs6022662
ebirs6022662
HLIrs6022662
Exacrs6022662
Varsomers6022662
Maprs6022662
PheGenIrs6022662
hapmaprs6022662
1000 genomesrs6022662
hgdprs6022662
ensemblrs6022662
gopubmedrs6022662
geneviewrs6022662
scholarrs6022662
googlers6022662
pharmgkbrs6022662
gwascentralrs6022662
openSNPrs6022662
23andMers6022662
23andMe allrs6022662
SNP Nexus

SNPshotrs6022662
SNPdbers6022662
MSV3drs6022662
GWAS Ctlgrs6022662
GMAF0.2548
Max Magnitude

Please note that this SNP is NOT associated with vitamin B12 deficiency. The original article was printed with a typo. Here is the correction: http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2683944/pdf/main.pdf. The correct SNP is rs602662.

GET Evidence
rs6022662
aa_change
aa_change_short
impact pharmacogenetic
qualified_impact Insufficiently evaluated pharmacogenetic
overall_frequency 0.335938
summary