rs6659553
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in complete genomics |
(T;T) | 0 | common in clinvar |
Make rs6659553(C;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 1 |
Position | 46189486 |
Gene | POMGNT1, TSPAN1 |
is a | snp |
is | mentioned by |
dbSNP | rs6659553 |
dbSNP (classic) | rs6659553 |
ClinGen | rs6659553 |
ebi | rs6659553 |
HLI | rs6659553 |
Exac | rs6659553 |
Gnomad | rs6659553 |
Varsome | rs6659553 |
LitVar | rs6659553 |
Map | rs6659553 |
PheGenI | rs6659553 |
Biobank | rs6659553 |
1000 genomes | rs6659553 |
hgdp | rs6659553 |
ensembl | rs6659553 |
geneview | rs6659553 |
scholar | rs6659553 |
rs6659553 | |
pharmgkb | rs6659553 |
gwascentral | rs6659553 |
openSNP | rs6659553 |
23andMe | rs6659553 |
SNPshot | rs6659553 |
SNPdbe | rs6659553 |
MSV3d | rs6659553 |
GWAS Ctlg | rs6659553 |
GMAF | 0.04821 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
ClinVar | |
---|---|
Risk | Rs6659553(C;C) |
Alt | Rs6659553(C;C) |
Reference | Rs6659553(T;T) |
Significance | Non-pathogenic |
Disease | not specified |
Variation | info |
Gene | POMGNT1 |
CLNDBN | not specified |
Reversed | 0 |
HGVS | NC_000001.10:g.46655158T>C |
CLNSRC | |
CLNACC | RCV000153758.3, |