rs57758506
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(A;A) | 0 | common in clinvar |
Make rs57758506(A;T) |
Make rs57758506(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 12 |
Position | 52949556 |
Gene | KRT8, KRT18 |
is a | snp |
is | mentioned by |
dbSNP | rs57758506 |
dbSNP (classic) | rs57758506 |
ClinGen | rs57758506 |
ebi | rs57758506 |
HLI | rs57758506 |
Exac | rs57758506 |
Gnomad | rs57758506 |
Varsome | rs57758506 |
LitVar | rs57758506 |
Map | rs57758506 |
PheGenI | rs57758506 |
Biobank | rs57758506 |
1000 genomes | rs57758506 |
hgdp | rs57758506 |
ensembl | rs57758506 |
geneview | rs57758506 |
scholar | rs57758506 |
rs57758506 | |
pharmgkb | rs57758506 |
gwascentral | rs57758506 |
openSNP | rs57758506 |
23andMe | rs57758506 |
SNPshot | rs57758506 |
SNPdbe | rs57758506 |
MSV3d | rs57758506 |
GWAS Ctlg | rs57758506 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs57758506(T;T) |
Alt | rs57758506(T;T) |
Reference | Rs57758506(A;A) |
Significance | Other |
Disease | Cirrhosis not provided |
Variation | info |
Gene | KRT8 KRT18 |
CLNDBN | Cirrhosis, cryptogenic Cirrhosis, noncryptogenic, susceptibility to not provided |
Reversed | 0 |
HGVS | NC_000012.11:g.53343340A>T |
CLNSRC | OMIM Allelic Variant UniProtKB (protein) |
CLNACC | RCV000015686.21, RCV000015687.2, RCV000056435.1, |