rs201845396
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs201845396(C;T) |
Make rs201845396(T;T) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | 18 |
Position | 31545856 |
Gene | DSG2, DSG2-AS1 |
is a | snp |
is | mentioned by |
dbSNP | rs201845396 |
dbSNP (classic) | rs201845396 |
ClinGen | rs201845396 |
ebi | rs201845396 |
HLI | rs201845396 |
Exac | rs201845396 |
Gnomad | rs201845396 |
Varsome | rs201845396 |
LitVar | rs201845396 |
Map | rs201845396 |
PheGenI | rs201845396 |
Biobank | rs201845396 |
1000 genomes | rs201845396 |
hgdp | rs201845396 |
ensembl | rs201845396 |
geneview | rs201845396 |
scholar | rs201845396 |
rs201845396 | |
pharmgkb | rs201845396 |
gwascentral | rs201845396 |
openSNP | rs201845396 |
23andMe | rs201845396 |
SNPshot | rs201845396 |
SNPdbe | rs201845396 |
MSV3d | rs201845396 |
GWAS Ctlg | rs201845396 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs201845396(G;G) rs201845396(T;T) |
Alt | rs201845396(G;G) rs201845396(T;T) |
Reference | Rs201845396(C;C) |
Significance | Probable-Pathogenic |
Disease | not specified not provided |
Variation | info |
Gene | DSG2-AS1 DSG2 |
CLNDBN | not specified not provided |
Reversed | 0 |
HGVS | NC_000018.9:g.29125819C>T |
CLNSRC | |
CLNACC | RCV000219803.1, RCV000489296.1, |