rs753824908
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs753824908(C;T) |
Make rs753824908(T;T) |
Reference | GRCh38.p2 38.2/144 |
Chromosome | 21 |
Position | 45504431 |
Gene | COL18A1, SLC19A1 |
is a | snp |
is | mentioned by |
dbSNP | rs753824908 |
dbSNP (classic) | rs753824908 |
ClinGen | rs753824908 |
ebi | rs753824908 |
HLI | rs753824908 |
Exac | rs753824908 |
Gnomad | rs753824908 |
Varsome | rs753824908 |
LitVar | rs753824908 |
Map | rs753824908 |
PheGenI | rs753824908 |
Biobank | rs753824908 |
1000 genomes | rs753824908 |
hgdp | rs753824908 |
ensembl | rs753824908 |
geneview | rs753824908 |
scholar | rs753824908 |
rs753824908 | |
pharmgkb | rs753824908 |
gwascentral | rs753824908 |
openSNP | rs753824908 |
23andMe | rs753824908 |
SNPshot | rs753824908 |
SNPdbe | rs753824908 |
MSV3d | rs753824908 |
GWAS Ctlg | rs753824908 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs753824908(T;T) |
Alt | rs753824908(T;T) |
Reference | Rs753824908(C;C) |
Significance | Probable-Pathogenic |
Disease | not provided |
Variation | info |
Gene | LOC101928717 COL18A1 |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000021.8:g.46924345C>T |
CLNSRC | |
CLNACC | RCV000171509.1, |