rs377138881
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs377138881(A;A) |
Make rs377138881(A;G) |
Reference | GRCh38.p2 38.2/146 |
Chromosome | 9 |
Position | 134824666 |
Gene | COL5A1, LOC101448202 |
is a | snp |
is | mentioned by |
dbSNP | rs377138881 |
dbSNP (classic) | rs377138881 |
ClinGen | rs377138881 |
ebi | rs377138881 |
HLI | rs377138881 |
Exac | rs377138881 |
Gnomad | rs377138881 |
Varsome | rs377138881 |
LitVar | rs377138881 |
Map | rs377138881 |
PheGenI | rs377138881 |
Biobank | rs377138881 |
1000 genomes | rs377138881 |
hgdp | rs377138881 |
ensembl | rs377138881 |
geneview | rs377138881 |
scholar | rs377138881 |
rs377138881 | |
pharmgkb | rs377138881 |
gwascentral | rs377138881 |
openSNP | rs377138881 |
23andMe | rs377138881 |
SNPshot | rs377138881 |
SNPdbe | rs377138881 |
MSV3d | rs377138881 |
GWAS Ctlg | rs377138881 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs377138881(A;A) |
Alt | rs377138881(A;A) |
Reference | Rs377138881(G;G) |
Significance | Probable-Pathogenic |
Disease | not provided |
Variation | info |
Gene | COL5A1 |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000009.11:g.137716512G>A |
CLNSRC | |
CLNACC | RCV000195865.1, |