rs749056160
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs749056160(C;T) |
Make rs749056160(T;T) |
Reference | GRCh38.p2 38.2/144 |
Chromosome | 8 |
Position | 125059395 |
Gene | KIAA0196, WASHC5 |
is a | snp |
is | mentioned by |
dbSNP | rs749056160 |
dbSNP (classic) | rs749056160 |
ClinGen | rs749056160 |
ebi | rs749056160 |
HLI | rs749056160 |
Exac | rs749056160 |
Gnomad | rs749056160 |
Varsome | rs749056160 |
LitVar | rs749056160 |
Map | rs749056160 |
PheGenI | rs749056160 |
Biobank | rs749056160 |
1000 genomes | rs749056160 |
hgdp | rs749056160 |
ensembl | rs749056160 |
geneview | rs749056160 |
scholar | rs749056160 |
rs749056160 | |
pharmgkb | rs749056160 |
gwascentral | rs749056160 |
openSNP | rs749056160 |
23andMe | rs749056160 |
SNPshot | rs749056160 |
SNPdbe | rs749056160 |
MSV3d | rs749056160 |
GWAS Ctlg | rs749056160 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs749056160(T;T) |
Alt | rs749056160(T;T) |
Reference | Rs749056160(C;C) |
Significance | Probable-Pathogenic |
Disease | not provided |
Variation | info |
Gene | KIAA0196 |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000008.10:g.126071637C>T |
CLNSRC | |
CLNACC | RCV000171420.1, |