rs2234921
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(A;A) | 0 | common in clinvar |
Make rs2234921(A;G) |
Make rs2234921(G;G) |
Reference | GRCh38.p2 38.2/144 |
Chromosome | 22 |
Position | 32801088 |
Gene | SYN3, TIMP3 |
is a | snp |
is | mentioned by |
dbSNP | rs2234921 |
dbSNP (classic) | rs2234921 |
ClinGen | rs2234921 |
ebi | rs2234921 |
HLI | rs2234921 |
Exac | rs2234921 |
Gnomad | rs2234921 |
Varsome | rs2234921 |
LitVar | rs2234921 |
Map | rs2234921 |
PheGenI | rs2234921 |
Biobank | rs2234921 |
1000 genomes | rs2234921 |
hgdp | rs2234921 |
ensembl | rs2234921 |
geneview | rs2234921 |
scholar | rs2234921 |
rs2234921 | |
pharmgkb | rs2234921 |
gwascentral | rs2234921 |
openSNP | rs2234921 |
23andMe | rs2234921 |
SNPshot | rs2234921 |
SNPdbe | rs2234921 |
MSV3d | rs2234921 |
GWAS Ctlg | rs2234921 |
Max Magnitude | 0 |
[PMID 25128867] Association of tissue inhibitor of metalloproteinase gene polymorphisms and unexplained recurrent spontaneous abortions in Han Chinese couples
ClinVar | |
---|---|
Risk | rs2234921(G;G) |
Alt | rs2234921(G;G) |
Reference | Rs2234921(A;A) |
Significance | Non-pathogenic |
Disease | Pseudoinflammatory fundus dystrophy |
Variation | info |
Gene | SYN3 TIMP3 |
CLNDBN | Pseudoinflammatory fundus dystrophy |
Reversed | 0 |
HGVS | NC_000022.10:g.33197074A>G |
CLNSRC | |
CLNACC | RCV000345010.1, |