rs7772593
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs7772593(C;C) |
Make rs7772593(C;T) |
Make rs7772593(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 6 |
Position | 105897182 |
is a | snp |
is | mentioned by |
dbSNP | rs7772593 |
dbSNP (classic) | rs7772593 |
ClinGen | rs7772593 |
ebi | rs7772593 |
HLI | rs7772593 |
Exac | rs7772593 |
Gnomad | rs7772593 |
Varsome | rs7772593 |
LitVar | rs7772593 |
Map | rs7772593 |
PheGenI | rs7772593 |
Biobank | rs7772593 |
1000 genomes | rs7772593 |
hgdp | rs7772593 |
ensembl | rs7772593 |
geneview | rs7772593 |
scholar | rs7772593 |
rs7772593 | |
pharmgkb | rs7772593 |
gwascentral | rs7772593 |
openSNP | rs7772593 |
23andMe | rs7772593 |
SNPshot | rs7772593 |
SNPdbe | rs7772593 |
MSV3d | rs7772593 |
GWAS Ctlg | rs7772593 |
GMAF | 0.1134 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
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[PMID 19922138] Analysis of FGGY as a risk factor for sporadic amyotrophic lateral sclerosis