Have questions? Visit https://www.reddit.com/r/SNPedia

rs6918152

From SNPedia

Orientationplus
Stabilizedplus
Make rs6918152(A;A)
Make rs6918152(A;G)
Make rs6918152(G;G)
ReferenceGRCh37 37.1/131
Chromosome6
Position542159
GeneEXOC2
is asnp
is mentioned by
dbSNPrs6918152
ebirs6918152
HLIrs6918152
Exacrs6918152
Varsomers6918152
Maprs6918152
PheGenIrs6918152
hapmaprs6918152
1000 genomesrs6918152
hgdprs6918152
ensemblrs6918152
gopubmedrs6918152
geneviewrs6918152
scholarrs6918152
googlers6918152
pharmgkbrs6918152
gwascentralrs6918152
openSNPrs6918152
23andMers6918152
23andMe allrs6918152
SNP Nexus

SNPshotrs6918152
SNPdbers6918152
MSV3drs6918152
GWAS Ctlgrs6918152
GMAF0.4766
Max Magnitude
? (A;A) (A;G) (G;G) 28
GWAS
SNP rs6918152
PubMedID [PMID 18483556OA-icon.png]
Condition Black vs. red hair color
Gene EXOC2
Risk Allele A
pValue 5.00E-007
OR 0.11
95% CI 0.07-0.15) increase in hair color scor




GET Evidence
rs6918152
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.445312
summary