rs373911488
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs373911488(A;A) |
Make rs373911488(A;G) |
Make rs373911488(G;G) |
Reference | GRCh38.p7 38.3/151 |
Chromosome | 10 |
Position | 104167627 |
Gene | CFAP43 |
is a | snp |
is | mentioned by |
dbSNP | rs373911488 |
dbSNP (classic) | rs373911488 |
ClinGen | rs373911488 |
ebi | rs373911488 |
HLI | rs373911488 |
Exac | rs373911488 |
Gnomad | rs373911488 |
Varsome | rs373911488 |
LitVar | rs373911488 |
Map | rs373911488 |
PheGenI | rs373911488 |
Biobank | rs373911488 |
1000 genomes | rs373911488 |
hgdp | rs373911488 |
ensembl | rs373911488 |
geneview | rs373911488 |
scholar | rs373911488 |
rs373911488 | |
pharmgkb | rs373911488 |
gwascentral | rs373911488 |
openSNP | rs373911488 |
23andMe | rs373911488 |
SNPshot | rs373911488 |
SNPdbe | rs373911488 |
MSV3d | rs373911488 |
GWAS Ctlg | rs373911488 |
Max Magnitude | 0 |
aka NM_025145.6(CFAP43):c.2802T>A or (p.Cys934Ter)
OMIM pathogenic variant