RS1126809 TYR
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What This Variant Does
"rs1126809 is a SNP in the TYR tyrosinase gene. This SNP is also known as R402Q (or, 1205G>
Associated Conditions
Oculocutaneous albinism type 1B
Temperature-sensitive oculocutaneous albinism type 1
Melanoma
cutaneous malignant
susceptibility to
8
SKIN/HAIR/EYE PIGMENTATION 3
LIGHT/DARK SKIN
Skin/hair/eye pigmentation 3
blue/green eyes
Oculocutaneous albinism type 1A
6 conditions
Autosomal recessive ocular albinism
Malignant tumor of breast
Oculocutaneous albinism type 1
GWAS Studies (20)
| Trait | Risk Allele | OR / Beta | P-value | Study |
|---|---|---|---|---|
| Sunburns | — | — | 4E-280 | PubMed |
| Eye color | G | OR: 0.29 | 2E-255 | PubMed |
| Cutaneous melanoma or hair colour | G | — | 4E-199 | PubMed |
| Low tan response | A | OR: 0.26 | 2E-172 | PubMed |
| Actinic keratosis (PheCode 702.1) | G | OR: 0.15 | 4E-171 | PubMed |
| Skin cancer | G | OR: 0.15 | 5E-165 | PubMed |
| Other non-epithelial cancer of skin (PheCode 172.2) | G | OR: 0.15 | 6E-138 | PubMed |
| Melanomas of skin, dx or hx (PheCode 172.1) | G | OR: 0.17 | 3E-114 | PubMed |
| Actinic keratosis (PheCode 702.1) | G | OR: 0.15 | 5E-100 | PubMed |
| Skin cancer | G | OR: 0.15 | 2E-99 | PubMed |
| Degenerative skin conditions and other dermatoses (PheCode 702) | G | OR: 0.11 | 1E-98 | PubMed |
| Neoplasm of uncertain behavior of skin (PheCode 173) | G | OR: 0.14 | 1E-97 | PubMed |
| Skin cancer | G | OR: 0.15 | 8E-96 | PubMed |
| Other non-epithelial cancer of skin (PheCode 172.2) | G | OR: 0.15 | 3E-88 | PubMed |
| Melanomas of skin, dx or hx (PheCode 172.1) | G | OR: 0.17 | 5E-87 | PubMed |
| Basal cell carcinoma (PheCode 172.21) | G | OR: 0.16 | 4E-79 | PubMed |
| Left eye overall retinal pigment epithelium thickness | A | OR: 0.16 | 7E-76 | PubMed |
| Skin cancer | G | OR: 0.15 | 1E-72 | PubMed |
| Neoplasm of uncertain behavior of skin (PheCode 173) | G | OR: 0.14 | 1E-72 | PubMed |
| Cutaneous malignant melanoma | A | OR: 1.2 | 4E-70 | PubMed |
Other Variants in TYR