rs2315122
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(A;A) | 0 | common on affy axiom data |
Make rs2315122(A;G) |
Make rs2315122(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | X |
Position | 154156369 |
Gene | OPN1LW |
is a | snp |
is | mentioned by |
dbSNP | rs2315122 |
dbSNP (classic) | rs2315122 |
ClinGen | rs2315122 |
ebi | rs2315122 |
HLI | rs2315122 |
Exac | rs2315122 |
Gnomad | rs2315122 |
Varsome | rs2315122 |
LitVar | rs2315122 |
Map | rs2315122 |
PheGenI | rs2315122 |
Biobank | rs2315122 |
1000 genomes | rs2315122 |
hgdp | rs2315122 |
ensembl | rs2315122 |
geneview | rs2315122 |
scholar | rs2315122 |
rs2315122 | |
pharmgkb | rs2315122 |
gwascentral | rs2315122 |
openSNP | rs2315122 |
23andMe | rs2315122 |
SNPshot | rs2315122 |
SNPdbe | rs2315122 |
MSV3d | rs2315122 |
GWAS Ctlg | rs2315122 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
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colorblindness https://www.23andme.com/you/community/thread/13594/