rs149645175
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs149645175(C;G) |
Make rs149645175(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 11 |
Position | 68448822 |
Gene | LRP5 |
is a | snp |
is | mentioned by |
dbSNP | rs149645175 |
dbSNP (classic) | rs149645175 |
ClinGen | rs149645175 |
ebi | rs149645175 |
HLI | rs149645175 |
Exac | rs149645175 |
Gnomad | rs149645175 |
Varsome | rs149645175 |
LitVar | rs149645175 |
Map | rs149645175 |
PheGenI | rs149645175 |
Biobank | rs149645175 |
1000 genomes | rs149645175 |
hgdp | rs149645175 |
ensembl | rs149645175 |
geneview | rs149645175 |
scholar | rs149645175 |
rs149645175 | |
pharmgkb | rs149645175 |
gwascentral | rs149645175 |
openSNP | rs149645175 |
23andMe | rs149645175 |
SNPshot | rs149645175 |
SNPdbe | rs149645175 |
MSV3d | rs149645175 |
GWAS Ctlg | rs149645175 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs149645175(G;G) rs149645175(T;T) |
Alt | rs149645175(G;G) rs149645175(T;T) |
Reference | Rs149645175(C;C) |
Significance | Pathogenic |
Disease | Osteoporosis with pseudoglioma |
Variation | info |
Gene | LRP5 |
CLNDBN | Osteoporosis with pseudoglioma |
Reversed | 0 |
HGVS | NC_000011.9:g.68216290C>T |
CLNSRC | OMIM Allelic Variant |
CLNACC | RCV000033260.4, |