rs762760856
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs762760856(A;A) |
Make rs762760856(A;T) |
Make rs762760856(T;T) |
Reference | GRCh38.p7 38.3/151 |
Chromosome | 3 |
Position | 113396528 |
Gene | CFAP44 |
is a | snp |
is | mentioned by |
dbSNP | rs762760856 |
dbSNP (classic) | rs762760856 |
ClinGen | rs762760856 |
ebi | rs762760856 |
HLI | rs762760856 |
Exac | rs762760856 |
Gnomad | rs762760856 |
Varsome | rs762760856 |
LitVar | rs762760856 |
Map | rs762760856 |
PheGenI | rs762760856 |
Biobank | rs762760856 |
1000 genomes | rs762760856 |
hgdp | rs762760856 |
ensembl | rs762760856 |
geneview | rs762760856 |
scholar | rs762760856 |
rs762760856 | |
pharmgkb | rs762760856 |
gwascentral | rs762760856 |
openSNP | rs762760856 |
23andMe | rs762760856 |
SNPshot | rs762760856 |
SNPdbe | rs762760856 |
MSV3d | rs762760856 |
GWAS Ctlg | rs762760856 |
Max Magnitude | 0 |
aka NM_001164496.1(CFAP44):c.1769T>A or (p.Leu590Gln)
OMIM pathogenic variant