rs267599193
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs267599193(C;T) |
Make rs267599193(T;T) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | 2 |
Position | 211713583 |
Gene | ERBB4 |
is a | snp |
is | mentioned by |
dbSNP | rs267599193 |
dbSNP (classic) | rs267599193 |
ClinGen | rs267599193 |
ebi | rs267599193 |
HLI | rs267599193 |
Exac | rs267599193 |
Gnomad | rs267599193 |
Varsome | rs267599193 |
LitVar | rs267599193 |
Map | rs267599193 |
PheGenI | rs267599193 |
Biobank | rs267599193 |
1000 genomes | rs267599193 |
hgdp | rs267599193 |
ensembl | rs267599193 |
geneview | rs267599193 |
scholar | rs267599193 |
rs267599193 | |
pharmgkb | rs267599193 |
gwascentral | rs267599193 |
openSNP | rs267599193 |
23andMe | rs267599193 |
SNPshot | rs267599193 |
SNPdbe | rs267599193 |
MSV3d | rs267599193 |
GWAS Ctlg | rs267599193 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs267599193(T;T) |
Alt | rs267599193(T;T) |
Reference | Rs267599193(C;C) |
Significance | Probable-Pathogenic |
Disease | Malignant melanoma |
Variation | info |
Gene | ERBB4 |
CLNDBN | Malignant melanoma |
Reversed | 0 |
HGVS | NC_000002.11:g.212578308C>T |
CLNSRC | |
CLNACC | RCV000435571.1, |