rs1006615
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs1006615(C;T) |
Make rs1006615(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 9 |
Position | 130433393 |
Gene | HMCN2, LOC107987134 |
is a | snp |
is | mentioned by |
dbSNP | rs1006615 |
dbSNP (classic) | rs1006615 |
ClinGen | rs1006615 |
ebi | rs1006615 |
HLI | rs1006615 |
Exac | rs1006615 |
Gnomad | rs1006615 |
Varsome | rs1006615 |
LitVar | rs1006615 |
Map | rs1006615 |
PheGenI | rs1006615 |
Biobank | rs1006615 |
1000 genomes | rs1006615 |
hgdp | rs1006615 |
ensembl | rs1006615 |
geneview | rs1006615 |
scholar | rs1006615 |
rs1006615 | |
pharmgkb | rs1006615 |
gwascentral | rs1006615 |
openSNP | rs1006615 |
23andMe | rs1006615 |
SNPshot | rs1006615 |
SNPdbe | rs1006615 |
MSV3d | rs1006615 |
GWAS Ctlg | rs1006615 |
GMAF | 0.3517 |
Max Magnitude | 0 |
[PMID 18936756] rs1006615 is associated with increased risk for schizophrenia in German and Scandinavian samples
ClinVar | |
---|---|
Risk | rs1006615(A;A) rs1006615(T;T) |
Alt | rs1006615(A;A) rs1006615(T;T) |
Reference | Rs1006615(C;C) |
Significance | Untested |
Disease | Malignant melanoma |
Variation | info |
Gene | HMCN2 |
CLNDBN | Malignant melanoma |
Reversed | 0 |
HGVS | NC_000009.12:g.130433393C>A |
CLNSRC | ClinVar |
CLNACC | RCV000068558.1, |