rs121912902
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs121912902(A;A) |
Make rs121912902(A;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 7 |
Position | 94424363 |
Gene | COL1A2 |
is a | snp |
is | mentioned by |
dbSNP | rs121912902 |
dbSNP (classic) | rs121912902 |
ClinGen | rs121912902 |
ebi | rs121912902 |
HLI | rs121912902 |
Exac | rs121912902 |
Gnomad | rs121912902 |
Varsome | rs121912902 |
LitVar | rs121912902 |
Map | rs121912902 |
PheGenI | rs121912902 |
Biobank | rs121912902 |
1000 genomes | rs121912902 |
hgdp | rs121912902 |
ensembl | rs121912902 |
geneview | rs121912902 |
scholar | rs121912902 |
rs121912902 | |
pharmgkb | rs121912902 |
gwascentral | rs121912902 |
openSNP | rs121912902 |
23andMe | rs121912902 |
SNPshot | rs121912902 |
SNPdbe | rs121912902 |
MSV3d | rs121912902 |
GWAS Ctlg | rs121912902 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs121912902(A;A) |
Alt | rs121912902(A;A) |
Reference | Rs121912902(G;G) |
Significance | Pathogenic |
Disease | Osteogenesis imperfecta |
Variation | info |
Gene | COL1A2 |
CLNDBN | Osteogenesis imperfecta, recessive perinatal lethal |
Reversed | 0 |
HGVS | NC_000007.13:g.94053675G>A |
CLNSRC | OMIM Allelic Variant |
CLNACC | RCV000018782.24, |