rs746993242
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(T;T) | 0 | common in clinvar |
Make rs746993242(G;G) |
Make rs746993242(G;T) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | 17 |
Position | 4901077 |
Gene | CHRNE, C17orf107 |
is a | snp |
is | mentioned by |
dbSNP | rs746993242 |
dbSNP (classic) | rs746993242 |
ClinGen | rs746993242 |
ebi | rs746993242 |
HLI | rs746993242 |
Exac | rs746993242 |
Gnomad | rs746993242 |
Varsome | rs746993242 |
LitVar | rs746993242 |
Map | rs746993242 |
PheGenI | rs746993242 |
Biobank | rs746993242 |
1000 genomes | rs746993242 |
hgdp | rs746993242 |
ensembl | rs746993242 |
geneview | rs746993242 |
scholar | rs746993242 |
rs746993242 | |
pharmgkb | rs746993242 |
gwascentral | rs746993242 |
openSNP | rs746993242 |
23andMe | rs746993242 |
SNPshot | rs746993242 |
SNPdbe | rs746993242 |
MSV3d | rs746993242 |
GWAS Ctlg | rs746993242 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs746993242(G;G) |
Alt | rs746993242(G;G) |
Reference | Rs746993242(T;T) |
Significance | Probable-Pathogenic |
Disease | not provided |
Variation | info |
Gene | C17orf107 CHRNE |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000017.10:g.4804372T>G |
CLNSRC | |
CLNACC | RCV000489085.1, |