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rs10078095

From SNPedia

Orientationplus
Stabilizedplus
Make rs10078095(C;C)
Make rs10078095(C;T)
Make rs10078095(T;T)
ReferenceGRCh38 38.1/141
Chromosome5
Position79460955
GeneHOMER1
is asnp
is mentioned by
dbSNPrs10078095
ebirs10078095
HLIrs10078095
Exacrs10078095
Varsomers10078095
Maprs10078095
PheGenIrs10078095
hapmaprs10078095
1000 genomesrs10078095
hgdprs10078095
ensemblrs10078095
gopubmedrs10078095
geneviewrs10078095
scholarrs10078095
googlers10078095
pharmgkbrs10078095
gwascentralrs10078095
openSNPrs10078095
23andMers10078095
23andMe allrs10078095
SNP Nexus

SNPshotrs10078095
SNPdbers10078095
MSV3drs10078095
GWAS Ctlgrs10078095
GMAF0.1827
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS
SNP rs10078095
PubMedID [PMID 18193045OA-icon.png]
Condition Height
Gene HOMER1
Risk Allele C
pValue 3.00E-006
OR 0.9
95% CI NR) cm talle



GET Evidence
rs10078095
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.265625
summary