rs539821357
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs539821357(A;A) |
Make rs539821357(A;C) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | 18 |
Position | 31546425 |
Gene | DSG2, DSG2-AS1 |
is a | snp |
is | mentioned by |
dbSNP | rs539821357 |
dbSNP (classic) | rs539821357 |
ClinGen | rs539821357 |
ebi | rs539821357 |
HLI | rs539821357 |
Exac | rs539821357 |
Gnomad | rs539821357 |
Varsome | rs539821357 |
LitVar | rs539821357 |
Map | rs539821357 |
PheGenI | rs539821357 |
Biobank | rs539821357 |
1000 genomes | rs539821357 |
hgdp | rs539821357 |
ensembl | rs539821357 |
geneview | rs539821357 |
scholar | rs539821357 |
rs539821357 | |
pharmgkb | rs539821357 |
gwascentral | rs539821357 |
openSNP | rs539821357 |
23andMe | rs539821357 |
SNPshot | rs539821357 |
SNPdbe | rs539821357 |
MSV3d | rs539821357 |
GWAS Ctlg | rs539821357 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs539821357(A;A) rs539821357(T;T) |
Alt | rs539821357(A;A) rs539821357(T;T) |
Reference | Rs539821357(C;C) |
Significance | Probable-Pathogenic |
Disease | not provided |
Variation | info |
Gene | DSG2-AS1 DSG2 |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000018.9:g.29126388C>A |
CLNSRC | |
CLNACC | RCV000431080.1, |