rs41274660
From SNPedia
Orientation | minus |
Stabilized | plus |
Make rs41274660(G;G) |
Make rs41274660(G;T) |
Make rs41274660(T;T) |
Reference | GRCh38.p2 38.2/144 |
Chromosome | 10 |
Position | 46046289 |
Gene | MSMB |
is a | snp |
is | mentioned by |
dbSNP | rs41274660 |
dbSNP (classic) | rs41274660 |
ClinGen | rs41274660 |
ebi | rs41274660 |
HLI | rs41274660 |
Exac | rs41274660 |
Gnomad | rs41274660 |
Varsome | rs41274660 |
LitVar | rs41274660 |
Map | rs41274660 |
PheGenI | rs41274660 |
Biobank | rs41274660 |
1000 genomes | rs41274660 |
hgdp | rs41274660 |
ensembl | rs41274660 |
geneview | rs41274660 |
scholar | rs41274660 |
rs41274660 | |
pharmgkb | rs41274660 |
gwascentral | rs41274660 |
openSNP | rs41274660 |
23andMe | rs41274660 |
SNPshot | rs41274660 |
SNPdbe | rs41274660 |
MSV3d | rs41274660 |
GWAS Ctlg | rs41274660 |
Max Magnitude | 0 |
[PMID 26240778] The rs10993994 in the proximal MSMB promoter region is a functional polymorphism in Asian Indian subjects