rs886041715
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Chromosome | 16 |
Position | 56192353 |
Gene | DKFZP434H168, GNAO1, LOC283856 |
is a | snp |
is | mentioned by |
dbSNP | rs886041715 |
dbSNP (classic) | rs886041715 |
ClinGen | rs886041715 |
ebi | rs886041715 |
HLI | rs886041715 |
Exac | rs886041715 |
Gnomad | rs886041715 |
Varsome | rs886041715 |
LitVar | rs886041715 |
Map | rs886041715 |
PheGenI | rs886041715 |
Biobank | rs886041715 |
1000 genomes | rs886041715 |
hgdp | rs886041715 |
ensembl | rs886041715 |
geneview | rs886041715 |
scholar | rs886041715 |
rs886041715 | |
pharmgkb | rs886041715 |
gwascentral | rs886041715 |
openSNP | rs886041715 |
23andMe | rs886041715 |
SNPshot | rs886041715 |
SNPdbe | rs886041715 |
MSV3d | rs886041715 |
GWAS Ctlg | rs886041715 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs886041715(C;C) rs886041715(T;T) |
Alt | rs886041715(C;C) rs886041715(T;T) |
Reference | Rs886041715(G;G) |
Significance | Pathogenic |
Disease | not specified not provided |
Variation | info |
Gene | DKFZP434H168 GNAO1 LOC283856 |
CLNDBN | not specified not provided |
Reversed | 0 |
HGVS | NC_000016.9:g.56226265G>C; NC_000016.9:g.56226265G>T |
CLNSRC | |
CLNACC | RCV000356569.1, RCV000486165.1, RCV000403784.1, |