rs535202189
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs535202189(C;T) |
Make rs535202189(T;T) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | 2 |
Position | 211673256 |
Gene | ERBB4 |
is a | snp |
is | mentioned by |
dbSNP | rs535202189 |
dbSNP (classic) | rs535202189 |
ClinGen | rs535202189 |
ebi | rs535202189 |
HLI | rs535202189 |
Exac | rs535202189 |
Gnomad | rs535202189 |
Varsome | rs535202189 |
LitVar | rs535202189 |
Map | rs535202189 |
PheGenI | rs535202189 |
Biobank | rs535202189 |
1000 genomes | rs535202189 |
hgdp | rs535202189 |
ensembl | rs535202189 |
geneview | rs535202189 |
scholar | rs535202189 |
rs535202189 | |
pharmgkb | rs535202189 |
gwascentral | rs535202189 |
openSNP | rs535202189 |
23andMe | rs535202189 |
SNPshot | rs535202189 |
SNPdbe | rs535202189 |
MSV3d | rs535202189 |
GWAS Ctlg | rs535202189 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs535202189(T;T) |
Alt | rs535202189(T;T) |
Reference | Rs535202189(C;C) |
Significance | Probable-Pathogenic |
Disease | Malignant melanoma |
Variation | info |
Gene | ERBB4 |
CLNDBN | Malignant melanoma |
Reversed | 0 |
HGVS | NC_000002.11:g.212537981C>T |
CLNSRC | |
CLNACC | RCV000431732.1, |