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rs770189

From SNPedia

Orientationminus
Stabilizedplus
Make rs770189(C;C)
Make rs770189(C;G)
Make rs770189(G;G)
ReferenceGRCh38 38.1/142
Chromosome5
Position88792622
GeneMEF2C
is asnp
is mentioned by
dbSNPrs770189
ebirs770189
HLIrs770189
Exacrs770189
Varsomers770189
Maprs770189
PheGenIrs770189
hapmaprs770189
1000 genomesrs770189
hgdprs770189
ensemblrs770189
gopubmedrs770189
geneviewrs770189
scholarrs770189
googlers770189
pharmgkbrs770189
gwascentralrs770189
openSNPrs770189
23andMers770189
23andMe allrs770189
SNP Nexus

SNPshotrs770189
SNPdbers770189
MSV3drs770189
GWAS Ctlgrs770189
GMAF0.4555
Max Magnitude
? (C;C) (C;G) (G;G) 28
GWAS
SNP rs770189
PubMedID [PMID 17903302OA-icon.png]
Condition Tonometry
Gene MEF2C
Risk Allele
pValue 3.00E-006
OR NA
95% CI



GET Evidence
rs770189
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.476562
summary