rs8192916
From SNPedia
Orientation | minus |
Stabilized | minus |
Make rs8192916(C;C) |
Make rs8192916(C;T) |
Make rs8192916(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 14 |
Position | 24635154 |
Gene | GZMB, LOC107984667 |
is a | snp |
is | mentioned by |
dbSNP | rs8192916 |
dbSNP (classic) | rs8192916 |
ClinGen | rs8192916 |
ebi | rs8192916 |
HLI | rs8192916 |
Exac | rs8192916 |
Gnomad | rs8192916 |
Varsome | rs8192916 |
LitVar | rs8192916 |
Map | rs8192916 |
PheGenI | rs8192916 |
Biobank | rs8192916 |
1000 genomes | rs8192916 |
hgdp | rs8192916 |
ensembl | rs8192916 |
geneview | rs8192916 |
scholar | rs8192916 |
rs8192916 | |
pharmgkb | rs8192916 |
gwascentral | rs8192916 |
openSNP | rs8192916 |
23andMe | rs8192916 |
SNPshot | rs8192916 |
SNPdbe | rs8192916 |
MSV3d | rs8192916 |
GWAS Ctlg | rs8192916 |
GMAF | 0.4931 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
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[PMID 23440692] A genetic variant in granzyme B is associated with progression of joint destruction in rheumatoid arthritis