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rs6941712

From SNPedia

Orientationplus
Stabilizedplus
Make rs6941712(C;C)
Make rs6941712(C;T)
Make rs6941712(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position130961070
GeneEPB41L2
is asnp
is mentioned by
dbSNPrs6941712
dbSNP (classic)rs6941712
ClinGenrs6941712
ebirs6941712
HLIrs6941712
Exacrs6941712
Gnomadrs6941712
Varsomers6941712
LitVarrs6941712
Maprs6941712
PheGenIrs6941712
Biobankrs6941712
1000 genomesrs6941712
hgdprs6941712
ensemblrs6941712
geneviewrs6941712
scholarrs6941712
googlers6941712
pharmgkbrs6941712
gwascentralrs6941712
openSNPrs6941712
23andMers6941712
SNPshotrs6941712
SNPdbers6941712
MSV3drs6941712
GWAS Ctlgrs6941712
GMAF0.2782
Max Magnitude0
? (C;C) (C;T) (T;T) 28


GWAS snp
PMID [PMID 22903471OA-icon.png]
Trait Lentiform nucleus volume
Title Genome-wide association identifies genetic variants associated with lentiform nucleus volume in N = 1345 young and elderly subjects.
Risk Allele C
P-val 5E-6
Odds Ratio 149.67 [NR] unit decrease