rs1131691651
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common/normal |
Make rs1131691651(C;T) |
Make rs1131691651(T;T) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | 2 |
Position | 71526343 |
Gene | DYSF |
is a | snp |
is | mentioned by |
dbSNP | rs1131691651 |
dbSNP (classic) | rs1131691651 |
ClinGen | rs1131691651 |
ebi | rs1131691651 |
HLI | rs1131691651 |
Exac | rs1131691651 |
Gnomad | rs1131691651 |
Varsome | rs1131691651 |
LitVar | rs1131691651 |
Map | rs1131691651 |
PheGenI | rs1131691651 |
Biobank | rs1131691651 |
1000 genomes | rs1131691651 |
hgdp | rs1131691651 |
ensembl | rs1131691651 |
geneview | rs1131691651 |
scholar | rs1131691651 |
rs1131691651 | |
pharmgkb | rs1131691651 |
gwascentral | rs1131691651 |
openSNP | rs1131691651 |
23andMe | rs1131691651 |
SNPshot | rs1131691651 |
SNPdbe | rs1131691651 |
MSV3d | rs1131691651 |
GWAS Ctlg | rs1131691651 |
Max Magnitude | 0 |
aka c.1177C>T (p.Gln393Ter)