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

rs6610953

From SNPedia

Orientationplus
Stabilizedplus
Make rs6610953(A;A)
Make rs6610953(A;G)
Make rs6610953(G;G)
ReferenceGRCh38 38.1/141
ChromosomeX
Position44540940
GeneFUNDC1
is asnp
is mentioned by
dbSNPrs6610953
ebirs6610953
HLIrs6610953
Exacrs6610953
Varsomers6610953
Maprs6610953
PheGenIrs6610953
hapmaprs6610953
1000 genomesrs6610953
hgdprs6610953
ensemblrs6610953
gopubmedrs6610953
geneviewrs6610953
scholarrs6610953
googlers6610953
pharmgkbrs6610953
gwascentralrs6610953
openSNPrs6610953
23andMers6610953
23andMe allrs6610953
SNP Nexus

SNPshotrs6610953
SNPdbers6610953
MSV3drs6610953
GWAS Ctlgrs6610953
GMAF0.1457
Max Magnitude
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 18957941OA-icon.png]
Trait Personality dimensions
Title Genome-wide association scan for five major dimensions of personality
Risk Allele G
P-val 0.000006
Odds Ratio 0.15 [NR] SD increase



GET Evidence
rs6610953
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.144444
summary