rs587776894
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs587776894(-;-) |
Make rs587776894(-;G) |
Make rs587776894(G;G) |
Reference | GRCh38.p7 38.3/151 |
Chromosome | 10 |
Position | 101030054 |
Gene | PDZD7, SFXN3 |
is a | snp |
is | mentioned by |
dbSNP | rs587776894 |
dbSNP (classic) | rs587776894 |
ClinGen | rs587776894 |
ebi | rs587776894 |
HLI | rs587776894 |
Exac | rs587776894 |
Gnomad | rs587776894 |
Varsome | rs587776894 |
LitVar | rs587776894 |
Map | rs587776894 |
PheGenI | rs587776894 |
Biobank | rs587776894 |
1000 genomes | rs587776894 |
hgdp | rs587776894 |
ensembl | rs587776894 |
geneview | rs587776894 |
scholar | rs587776894 |
rs587776894 | |
pharmgkb | rs587776894 |
gwascentral | rs587776894 |
openSNP | rs587776894 |
23andMe | rs587776894 |
SNPshot | rs587776894 |
SNPdbe | rs587776894 |
MSV3d | rs587776894 |
GWAS Ctlg | rs587776894 |
Max Magnitude | 0 |
aka NM_001195263.1(PDZD7):c.166dupC or (p.Arg56Profs)
OMIM pathogenic variant