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rs16982743

From SNPedia

Orientationplus
Stabilizedplus
Make rs16982743(A;A)
Make rs16982743(A;G)
Make rs16982743(G;G)
ReferenceGRCh38 38.1/141
Chromosome19
Position51501649
GeneSIGLEC12
is asnp
is mentioned by
dbSNPrs16982743
ebirs16982743
HLIrs16982743
Exacrs16982743
Varsomers16982743
Maprs16982743
PheGenIrs16982743
hapmaprs16982743
1000 genomesrs16982743
hgdprs16982743
ensemblrs16982743
gopubmedrs16982743
geneviewrs16982743
scholarrs16982743
googlers16982743
pharmgkbrs16982743
gwascentralrs16982743
openSNPrs16982743
23andMers16982743
23andMe allrs16982743
SNP Nexus

SNPshotrs16982743
SNPdbers16982743
MSV3drs16982743
GWAS Ctlgrs16982743
GMAF0.1873
Max Magnitude
? (A;A) (A;G) (G;G) 28
[PMID 23690342OA-icon.png] Pharmacogenomic Association of Nonsynonymous SNPs in SIGLEC12, A1BG, and the Selectin Region and Cardiovascular Outcomes


[PMID 19200524OA-icon.png] A genome-wide survey of the prevalence and evolutionary forces acting on human nonsense SNPs.