rs6496932
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs6496932(A;A) |
Make rs6496932(A;C) |
Make rs6496932(C;C) |
Reference | GRCh38 38.1/141 |
Chromosome | 15 |
Position | 85282336 |
Gene | LOC642935 |
is a | snp |
is | mentioned by |
dbSNP | rs6496932 |
dbSNP (classic) | rs6496932 |
ClinGen | rs6496932 |
ebi | rs6496932 |
HLI | rs6496932 |
Exac | rs6496932 |
Gnomad | rs6496932 |
Varsome | rs6496932 |
LitVar | rs6496932 |
Map | rs6496932 |
PheGenI | rs6496932 |
Biobank | rs6496932 |
1000 genomes | rs6496932 |
hgdp | rs6496932 |
ensembl | rs6496932 |
geneview | rs6496932 |
scholar | rs6496932 |
rs6496932 | |
pharmgkb | rs6496932 |
gwascentral | rs6496932 |
openSNP | rs6496932 |
23andMe | rs6496932 |
SNPshot | rs6496932 |
SNPdbe | rs6496932 |
MSV3d | rs6496932 |
GWAS Ctlg | rs6496932 |
GMAF | 0.3108 |
Max Magnitude | 0 |
? | (A;A) (A;C) (C;C) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 20719862] |
Trait | |
Title | New loci associated with central cornea thickness include COL5A1, AKAP13 and AVGR8 |
Risk Allele | C |
P-val | 1E-8 |
Odds Ratio | 0.13 [0.09-0.18] unit increase |
[PMID 21984434] Identification of four novel variants that influence central corneal thickness in multi-ethnic Asian populations.
GWAS snp | |
---|---|
PMID | [PMID 23291589![]() |
Trait | Corneal structure |
Title | Genome-wide association analyses identify multiple loci associated with central corneal thickness and keratoconus. |
Risk Allele | A |
P-val | 7E-13 |
Odds Ratio | .11 [0.071-0.149] unit decrease |
Categories:
- Is a snp
- In dbSNP
- SNPs on chromosome 15
- Has genotype
- Has population
- On chip 23andMe v1
- On chip 23andMe v2
- On chip 23andMe v3
- On chip 23andMe v4
- On chip Affy GenomeWide 6
- On chip Ancestry v2
- On chip FTDNA2
- On chip FTDNA
- On chip HumanOmni1Quad
- On chip Illumina Human 1M
- On chip 23andMe v5
- On chip Ancestry v2c
- On chip Ancestry v2d