rs755303686
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs755303686(C;G) |
Make rs755303686(G;G) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | 17 |
Position | 4899385 |
Gene | CHRNE, C17orf107 |
is a | snp |
is | mentioned by |
dbSNP | rs755303686 |
dbSNP (classic) | rs755303686 |
ClinGen | rs755303686 |
ebi | rs755303686 |
HLI | rs755303686 |
Exac | rs755303686 |
Gnomad | rs755303686 |
Varsome | rs755303686 |
LitVar | rs755303686 |
Map | rs755303686 |
PheGenI | rs755303686 |
Biobank | rs755303686 |
1000 genomes | rs755303686 |
hgdp | rs755303686 |
ensembl | rs755303686 |
geneview | rs755303686 |
scholar | rs755303686 |
rs755303686 | |
pharmgkb | rs755303686 |
gwascentral | rs755303686 |
openSNP | rs755303686 |
23andMe | rs755303686 |
SNPshot | rs755303686 |
SNPdbe | rs755303686 |
MSV3d | rs755303686 |
GWAS Ctlg | rs755303686 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs755303686(G;G) |
Alt | rs755303686(G;G) |
Reference | Rs755303686(C;C) |
Significance | Pathogenic |
Disease | not provided |
Variation | info |
Gene | C17orf107 CHRNE |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000017.10:g.4802680C>G |
CLNSRC | |
CLNACC | RCV000483785.1, |