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rs976683

From SNPedia

Orientationminus
Stabilizedminus
Make rs976683(A;A)
Make rs976683(A;G)
Make rs976683(G;G)
ReferenceGRCh38 38.1/141
Chromosome3
Position173767581
GeneNLGN1
is asnp
is mentioned by
dbSNPrs976683
ebirs976683
HLIrs976683
Exacrs976683
Varsomers976683
Maprs976683
PheGenIrs976683
hapmaprs976683
1000 genomesrs976683
hgdprs976683
ensemblrs976683
gopubmedrs976683
geneviewrs976683
scholarrs976683
googlers976683
pharmgkbrs976683
gwascentralrs976683
openSNPrs976683
23andMers976683
23andMe allrs976683
SNP Nexus

SNPshotrs976683
SNPdbers976683
MSV3drs976683
GWAS Ctlgrs976683
GMAF0.4601
Max Magnitude
? (A;A) (A;G) (G;G) 28
[PMID 23929743OA-icon.png] Genome-Wide Analysis of Blood Pressure Variability and Ischemic Stroke


[PMID 20070850OA-icon.png] Genome-wide association study confirms SNPs in SNCA and the MAPT region as common risk factors for Parkinson disease.