rs876657565
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs876657565(C;T) |
Make rs876657565(T;T) |
Reference | GRCh38.p7 38.3/149 |
Chromosome | 1 |
Position | 3396583 |
Gene | PRDM16 |
is a | snp |
is | mentioned by |
dbSNP | rs876657565 |
dbSNP (classic) | rs876657565 |
ClinGen | rs876657565 |
ebi | rs876657565 |
HLI | rs876657565 |
Exac | rs876657565 |
Gnomad | rs876657565 |
Varsome | rs876657565 |
LitVar | rs876657565 |
Map | rs876657565 |
PheGenI | rs876657565 |
Biobank | rs876657565 |
1000 genomes | rs876657565 |
hgdp | rs876657565 |
ensembl | rs876657565 |
geneview | rs876657565 |
scholar | rs876657565 |
rs876657565 | |
pharmgkb | rs876657565 |
gwascentral | rs876657565 |
openSNP | rs876657565 |
23andMe | rs876657565 |
SNPshot | rs876657565 |
SNPdbe | rs876657565 |
MSV3d | rs876657565 |
GWAS Ctlg | rs876657565 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs876657565(T;T) |
Alt | rs876657565(T;T) |
Reference | Rs876657565(C;C) |
Significance | Probable-non-pathogenic |
Disease | not specified |
Variation | info |
Gene | PRDM16 |
CLNDBN | not specified |
Reversed | 0 |
HGVS | NC_000001.10:g.3313147C>T |
CLNSRC | |
CLNACC | RCV000488452.1, |