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rs6983473

From SNPedia

Orientationplus
Stabilizedplus
Make rs6983473(A;A)
Make rs6983473(A;T)
Make rs6983473(T;T)
ReferenceGRCh38 38.1/141
Chromosome8
Position28048371
GeneNUGGC
is asnp
is mentioned by
dbSNPrs6983473
dbSNP (classic)rs6983473
ClinGenrs6983473
ebirs6983473
HLIrs6983473
Exacrs6983473
Gnomadrs6983473
Varsomers6983473
LitVarrs6983473
Maprs6983473
PheGenIrs6983473
Biobankrs6983473
1000 genomesrs6983473
hgdprs6983473
ensemblrs6983473
geneviewrs6983473
scholarrs6983473
googlers6983473
pharmgkbrs6983473
gwascentralrs6983473
openSNPrs6983473
23andMers6983473
SNPshotrs6983473
SNPdbers6983473
MSV3drs6983473
GWAS Ctlgrs6983473
GMAF0.3356
Max Magnitude0
? (A;A) (A;T) (T;T) 28


GWAS snp
PMID [PMID 23247143OA-icon.png]
Trait Cardiac Troponin-T levels
Title Association of genome-wide variation with highly sensitive cardiac troponin-T levels in European americans and blacks: a meta-analysis from atherosclerosis risk in communities and cardiovascular health studies.
Risk Allele A
P-val 4E-6
Odds Ratio .04 [0.02-0.06] ug/L decrease