rs377406897
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs377406897(C;T) |
Make rs377406897(T;T) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | 1 |
Position | 11974738 |
Gene | PLOD1 |
is a | snp |
is | mentioned by |
dbSNP | rs377406897 |
dbSNP (classic) | rs377406897 |
ClinGen | rs377406897 |
ebi | rs377406897 |
HLI | rs377406897 |
Exac | rs377406897 |
Gnomad | rs377406897 |
Varsome | rs377406897 |
LitVar | rs377406897 |
Map | rs377406897 |
PheGenI | rs377406897 |
Biobank | rs377406897 |
1000 genomes | rs377406897 |
hgdp | rs377406897 |
ensembl | rs377406897 |
geneview | rs377406897 |
scholar | rs377406897 |
rs377406897 | |
pharmgkb | rs377406897 |
gwascentral | rs377406897 |
openSNP | rs377406897 |
23andMe | rs377406897 |
SNPshot | rs377406897 |
SNPdbe | rs377406897 |
MSV3d | rs377406897 |
GWAS Ctlg | rs377406897 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs377406897(T;T) |
Alt | rs377406897(T;T) |
Reference | Rs377406897(C;C) |
Significance | Probable-Pathogenic |
Disease | not provided |
Variation | info |
Gene | PLOD1 |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000001.10:g.12034795C>T |
CLNSRC | |
CLNACC | RCV000479022.1, |