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rs13289

From SNPedia

Orientationminus
Stabilizedminus
Make rs13289(C;C)
Make rs13289(C;G)
Make rs13289(G;G)
ReferenceGRCh38 38.1/141
Chromosome5
Position33986304
GeneSLC45A2
is asnp
is mentioned by
dbSNPrs13289
ebirs13289
HLIrs13289
Exacrs13289
Varsomers13289
Maprs13289
PheGenIrs13289
hapmaprs13289
1000 genomesrs13289
hgdprs13289
ensemblrs13289
gopubmedrs13289
geneviewrs13289
scholarrs13289
googlers13289
pharmgkbrs13289
gwascentralrs13289
openSNPrs13289
23andMers13289
23andMe allrs13289
SNP Nexus

SNPshotrs13289
SNPdbers13289
MSV3drs13289
GWAS Ctlgrs13289
GMAF0.4582
Max Magnitude
? (C;C) (C;G) (G;G) 28
OMIM227240
DescSKIN/HAIR/EYE PIGMENTATION, VARIATION IN, 5; SHEP5
Variant
Relatedalso
OMIM606202
DescSOLUTE CARRIER FAMILY 45, MEMBER 2; SLC45A2
Variant
Relatedalso


[PMID 17358008] Promoter polymorphisms in the MATP (SLC45A2) gene are associated with normal human skin color variation.


[PMID 18483556OA-icon.png] A genome-wide association study identifies novel alleles associated with hair color and skin pigmentation.


[PMID 19340012OA-icon.png] Genome-wide association study of tanning phenotype in a population of European ancestry.


[PMID 19384953OA-icon.png] Genetic variants in pigmentation genes, pigmentary phenotypes, and risk of skin cancer in Caucasians.