rs781134478
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(T;T) | 0 | common in clinvar |
Make rs781134478(G;G) |
Make rs781134478(G;T) |
Reference | GRCh38.p2 38.2/144 |
Chromosome | 15 |
Position | 30904756 |
Gene | FAN1 |
is a | snp |
is | mentioned by |
dbSNP | rs781134478 |
dbSNP (classic) | rs781134478 |
ClinGen | rs781134478 |
ebi | rs781134478 |
HLI | rs781134478 |
Exac | rs781134478 |
Gnomad | rs781134478 |
Varsome | rs781134478 |
LitVar | rs781134478 |
Map | rs781134478 |
PheGenI | rs781134478 |
Biobank | rs781134478 |
1000 genomes | rs781134478 |
hgdp | rs781134478 |
ensembl | rs781134478 |
geneview | rs781134478 |
scholar | rs781134478 |
rs781134478 | |
pharmgkb | rs781134478 |
gwascentral | rs781134478 |
openSNP | rs781134478 |
23andMe | rs781134478 |
SNPshot | rs781134478 |
SNPdbe | rs781134478 |
MSV3d | rs781134478 |
GWAS Ctlg | rs781134478 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs781134478(G;G) |
Alt | rs781134478(G;G) |
Reference | Rs781134478(T;T) |
Significance | Probable-Pathogenic |
Disease | not provided |
Variation | info |
Gene | FAN1 |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000015.9:g.31196959T>G |
CLNSRC | |
CLNACC | RCV000171228.1, |