rs190543052
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs190543052(G;G) |
Make rs190543052(G;T) |
Make rs190543052(T;T) |
Reference | GRCh38.p2 38.2/147 |
Chromosome | 7 |
Position | 121136045 |
Gene | CPED1 |
is a | snp |
is | mentioned by |
dbSNP | rs190543052 |
dbSNP (classic) | rs190543052 |
ClinGen | rs190543052 |
ebi | rs190543052 |
HLI | rs190543052 |
Exac | rs190543052 |
Gnomad | rs190543052 |
Varsome | rs190543052 |
LitVar | rs190543052 |
Map | rs190543052 |
PheGenI | rs190543052 |
Biobank | rs190543052 |
1000 genomes | rs190543052 |
hgdp | rs190543052 |
ensembl | rs190543052 |
geneview | rs190543052 |
scholar | rs190543052 |
rs190543052 | |
pharmgkb | rs190543052 |
gwascentral | rs190543052 |
openSNP | rs190543052 |
23andMe | rs190543052 |
SNPshot | rs190543052 |
SNPdbe | rs190543052 |
MSV3d | rs190543052 |
GWAS Ctlg | rs190543052 |
Max Magnitude | 0 |
C7orf58 SNP; one of five used in genetic risk score for lifetime prevalence of femoral fracture in Japanese males.[PMID 26462479]