rs780798708
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs780798708(-;-) |
Make rs780798708(-;AT) |
Make rs780798708(AT;AT) |
Reference | GRCh38.p7 38.3/151 |
Chromosome | 3 |
Position | 113380945 |
Gene | CFAP44 |
is a | snp |
is | mentioned by |
dbSNP | rs780798708 |
dbSNP (classic) | rs780798708 |
ClinGen | rs780798708 |
ebi | rs780798708 |
HLI | rs780798708 |
Exac | rs780798708 |
Gnomad | rs780798708 |
Varsome | rs780798708 |
LitVar | rs780798708 |
Map | rs780798708 |
PheGenI | rs780798708 |
Biobank | rs780798708 |
1000 genomes | rs780798708 |
hgdp | rs780798708 |
ensembl | rs780798708 |
geneview | rs780798708 |
scholar | rs780798708 |
rs780798708 | |
pharmgkb | rs780798708 |
gwascentral | rs780798708 |
openSNP | rs780798708 |
23andMe | rs780798708 |
SNPshot | rs780798708 |
SNPdbe | rs780798708 |
MSV3d | rs780798708 |
GWAS Ctlg | rs780798708 |
Max Magnitude | 0 |
aka NM_018338.3(CFAP44):c.2005_2006delAT or (p.Met669Valfs)
OMIM pathogenic variant