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

rs6462411

From SNPedia

Orientationplus
Stabilizedplus
Make rs6462411(C;C)
Make rs6462411(C;T)
Make rs6462411(T;T)
ReferenceGRCh38 38.1/141
Chromosome7
Position3875932
GeneSDK1
is asnp
is mentioned by
dbSNPrs6462411
ebirs6462411
HLIrs6462411
Exacrs6462411
Varsomers6462411
Maprs6462411
PheGenIrs6462411
hapmaprs6462411
1000 genomesrs6462411
hgdprs6462411
ensemblrs6462411
gopubmedrs6462411
geneviewrs6462411
scholarrs6462411
googlers6462411
pharmgkbrs6462411
gwascentralrs6462411
openSNPrs6462411
23andMers6462411
23andMe allrs6462411
SNP Nexus

SNPshotrs6462411
SNPdbers6462411
MSV3drs6462411
GWAS Ctlgrs6462411
GMAF0.286
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 19197348OA-icon.png]
Trait Quantitative traits
Title Genome-wide association studies in an isolated founder population from the Pacific Island of Kosrae
Risk Allele C
P-val 0.000001
Odds Ratio 0.36 [NR] mIU/L decrease


GET Evidence
rs6462411
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.304688
summary