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rs62408925

From SNPedia

Orientationplus
Stabilizedplus
Make rs62408925(C;C)
Make rs62408925(C;T)
Make rs62408925(T;T)
ReferenceGRCh38 38.1/141
Chromosome3
Position137071697
is asnp
is mentioned by
dbSNPrs62408925
ebirs62408925
HLIrs62408925
Exacrs62408925
Varsomers62408925
Maprs62408925
PheGenIrs62408925
hapmaprs62408925
1000 genomesrs62408925
hgdprs62408925
ensemblrs62408925
gopubmedrs62408925
geneviewrs62408925
scholarrs62408925
googlers62408925
pharmgkbrs62408925
gwascentralrs62408925
openSNPrs62408925
23andMers62408925
23andMe allrs62408925
SNP Nexus

SNPshotrs62408925
SNPdbers62408925
MSV3drs62408925
GWAS Ctlgrs62408925
GMAF0.1717
Max Magnitude
OMIM603933
DescMICROVASCULAR COMPLICATIONS OF DIABETES, SUSCEPTIBILITY TO, 1; MVCD1
Variant
Relatedalso



GET Evidence
rs62408925
aa_change
aa_change_short
impact pharmacogenetic
qualified_impact Insufficiently evaluated pharmacogenetic
overall_frequency 0.148438
summary