rs7164902
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs7164902(A;A) |
Make rs7164902(A;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 15 |
Position | 34258881 |
Gene | SLC12A6 |
is a | snp |
is | mentioned by |
dbSNP | rs7164902 |
dbSNP (classic) | rs7164902 |
ClinGen | rs7164902 |
ebi | rs7164902 |
HLI | rs7164902 |
Exac | rs7164902 |
Gnomad | rs7164902 |
Varsome | rs7164902 |
LitVar | rs7164902 |
Map | rs7164902 |
PheGenI | rs7164902 |
Biobank | rs7164902 |
1000 genomes | rs7164902 |
hgdp | rs7164902 |
ensembl | rs7164902 |
geneview | rs7164902 |
scholar | rs7164902 |
rs7164902 | |
pharmgkb | rs7164902 |
gwascentral | rs7164902 |
openSNP | rs7164902 |
23andMe | rs7164902 |
SNPshot | rs7164902 |
SNPdbe | rs7164902 |
MSV3d | rs7164902 |
GWAS Ctlg | rs7164902 |
GMAF | 0.2704 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
[PMID 21245421] Genetic Factors Underlying the Risk of Thalidomide-Related Neuropathy in Patients With Multiple Myeloma
ClinVar | |
---|---|
Risk | rs7164902(A;A) |
Alt | rs7164902(A;A) |
Reference | Rs7164902(G;G) |
Significance | Non-pathogenic |
Disease | not specified Andermann syndrome |
Variation | info |
Gene | SLC12A6 |
CLNDBN | not specified Andermann syndrome |
Reversed | 0 |
HGVS | NC_000015.9:g.34551082G>A |
CLNSRC | ClinVar University of Chicago |
CLNACC | RCV000147488.2, RCV000271997.1, |