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

rs12979618

From SNPedia

Orientationplus
Stabilizedplus
Make rs12979618(G;G)
Make rs12979618(G;T)
Make rs12979618(T;T)
ReferenceGRCh38 38.1/141
Chromosome19
Position38269930
GeneSPINT2
is asnp
is mentioned by
dbSNPrs12979618
ebirs12979618
HLIrs12979618
Exacrs12979618
Varsomers12979618
Maprs12979618
PheGenIrs12979618
hapmaprs12979618
1000 genomesrs12979618
hgdprs12979618
ensemblrs12979618
gopubmedrs12979618
geneviewrs12979618
scholarrs12979618
googlers12979618
pharmgkbrs12979618
gwascentralrs12979618
openSNPrs12979618
23andMers12979618
23andMe allrs12979618
SNP Nexus

SNPshotrs12979618
SNPdbers12979618
MSV3drs12979618
GWAS Ctlgrs12979618
Max Magnitude

[PMID 25233462OA-icon.png] IL28B Gene Polymorphism SNP rs8099917 Genotype GG Is Associated with HTLV-1-Associated Myelopathy/Tropical Spastic Paraparesis (HAM/TSP) in HTLV-1 Carriers