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rs6951651

From SNPedia

Orientationplus
Stabilizedplus
Make rs6951651(C;C)
Make rs6951651(C;G)
Make rs6951651(G;G)
ReferenceGRCh38 38.1/141
Chromosome7
Position103903456
GeneRELN
is asnp
is mentioned by
dbSNPrs6951651
dbSNP (old)rs6951651
ClinGenrs6951651
ebirs6951651
HLIrs6951651
Exacrs6951651
Gnomadrs6951651
Varsomers6951651
Maprs6951651
PheGenIrs6951651
Biobankrs6951651
1000 genomesrs6951651
hgdprs6951651
ensemblrs6951651
gopubmedrs6951651
geneviewrs6951651
scholarrs6951651
googlers6951651
pharmgkbrs6951651
gwascentralrs6951651
openSNPrs6951651
23andMers6951651
23andMe allrs6951651
SNP Nexus

SNPshotrs6951651
SNPdbers6951651
MSV3drs6951651
GWAS Ctlgrs6951651
GMAF0.4697
Max Magnitude
? (C;C) (C;G) (G;G) 28


GET Evidence
rs6951651
aa_change
aa_change_short
impact pharmacogenetic
qualified_impact Insufficiently evaluated pharmacogenetic
overall_frequency 0.579365
summary