rs10139154
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs10139154(C;C) |
Make rs10139154(C;T) |
Make rs10139154(T;T) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | 14 |
Position | 30678292 |
Gene | SCFD1 |
is a | snp |
is | mentioned by |
dbSNP | rs10139154 |
dbSNP (classic) | rs10139154 |
ClinGen | rs10139154 |
ebi | rs10139154 |
HLI | rs10139154 |
Exac | rs10139154 |
Gnomad | rs10139154 |
Varsome | rs10139154 |
LitVar | rs10139154 |
Map | rs10139154 |
PheGenI | rs10139154 |
Biobank | rs10139154 |
1000 genomes | rs10139154 |
hgdp | rs10139154 |
ensembl | rs10139154 |
geneview | rs10139154 |
scholar | rs10139154 |
rs10139154 | |
pharmgkb | rs10139154 |
gwascentral | rs10139154 |
openSNP | rs10139154 |
23andMe | rs10139154 |
SNPshot | rs10139154 |
SNPdbe | rs10139154 |
MSV3d | rs10139154 |
GWAS Ctlg | rs10139154 |
Max Magnitude | 0 |
[PMID 29260601] An association study between SCFD1 rs10139154 variant and amyotrophic lateral sclerosis in a Chinese cohort.