rs4536103
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(A;A) | 0 | common in clinvar |
Make rs4536103(A;G) |
Make rs4536103(G;G) |
Reference | GRCh38.p2 38.2/147 |
Chromosome | 10 |
Position | 69572448 |
Gene | LOC101929021, NEUROG3 |
is a | snp |
is | mentioned by |
dbSNP | rs4536103 |
dbSNP (classic) | rs4536103 |
ClinGen | rs4536103 |
ebi | rs4536103 |
HLI | rs4536103 |
Exac | rs4536103 |
Gnomad | rs4536103 |
Varsome | rs4536103 |
LitVar | rs4536103 |
Map | rs4536103 |
PheGenI | rs4536103 |
Biobank | rs4536103 |
1000 genomes | rs4536103 |
hgdp | rs4536103 |
ensembl | rs4536103 |
geneview | rs4536103 |
scholar | rs4536103 |
rs4536103 | |
pharmgkb | rs4536103 |
gwascentral | rs4536103 |
openSNP | rs4536103 |
23andMe | rs4536103 |
SNPshot | rs4536103 |
SNPdbe | rs4536103 |
MSV3d | rs4536103 |
GWAS Ctlg | rs4536103 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
[PMID 26343869] Genome-wide association study on progression of carotid artery intima media thickness over 10 years in a Chinese cohort.
ClinVar | |
---|---|
Risk | rs4536103(G;G) |
Alt | rs4536103(G;G) |
Reference | Rs4536103(A;A) |
Significance | Other |
Disease | not specified |
Variation | info |
Gene | NEUROG3 |
CLNDBN | not specified |
Reversed | 0 |
HGVS | NC_000010.10:g.71332204A>G |
CLNSRC | UniProtKB (protein) |
CLNACC | RCV000117780.2, |