rs374828868
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs374828868(A;A) |
Make rs374828868(A;G) |
Reference | GRCh38.p7 38.3/151 |
Chromosome | 8 |
Position | 98148852 |
Gene | POP1 |
is a | snp |
is | mentioned by |
dbSNP | rs374828868 |
dbSNP (classic) | rs374828868 |
ClinGen | rs374828868 |
ebi | rs374828868 |
HLI | rs374828868 |
Exac | rs374828868 |
Gnomad | rs374828868 |
Varsome | rs374828868 |
LitVar | rs374828868 |
Map | rs374828868 |
PheGenI | rs374828868 |
Biobank | rs374828868 |
1000 genomes | rs374828868 |
hgdp | rs374828868 |
ensembl | rs374828868 |
geneview | rs374828868 |
scholar | rs374828868 |
rs374828868 | |
pharmgkb | rs374828868 |
gwascentral | rs374828868 |
openSNP | rs374828868 |
23andMe | rs374828868 |
SNPshot | rs374828868 |
SNPdbe | rs374828868 |
MSV3d | rs374828868 |
GWAS Ctlg | rs374828868 |
Max Magnitude | 0 |
aka NM_001145860.1(POP1):c.1748G>A or (p.Gly583Glu)
OMIM pathogenic variant