rs16862847
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(A;A) | 0 | common in clinvar |
Make rs16862847(A;G) |
Make rs16862847(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 2 |
Position | 174764872 |
Gene | CHRNA1 |
is a | snp |
is | mentioned by |
dbSNP | rs16862847 |
dbSNP (classic) | rs16862847 |
ClinGen | rs16862847 |
ebi | rs16862847 |
HLI | rs16862847 |
Exac | rs16862847 |
Gnomad | rs16862847 |
Varsome | rs16862847 |
LitVar | rs16862847 |
Map | rs16862847 |
PheGenI | rs16862847 |
Biobank | rs16862847 |
1000 genomes | rs16862847 |
hgdp | rs16862847 |
ensembl | rs16862847 |
geneview | rs16862847 |
scholar | rs16862847 |
rs16862847 | |
pharmgkb | rs16862847 |
gwascentral | rs16862847 |
openSNP | rs16862847 |
23andMe | rs16862847 |
SNPshot | rs16862847 |
SNPdbe | rs16862847 |
MSV3d | rs16862847 |
GWAS Ctlg | rs16862847 |
GMAF | 0.1093 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs16862847(G;G) |
Alt | rs16862847(G;G) |
Reference | Rs16862847(A;A) |
Significance | Probable-non-pathogenic |
Disease | not specified |
Variation | info |
Gene | CHRNA1 |
CLNDBN | not specified |
Reversed | 1 |
HGVS | NC_000002.11:g.175629600T>C |
CLNSRC | |
CLNACC | RCV000249329.1, |