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rs35391

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in complete genomics
Make rs35391(C;T)
Make rs35391(T;T)
ReferenceGRCh38 38.1/141
Chromosome5
Position33955568
GeneSLC45A2
is asnp
is mentioned by
dbSNPrs35391
ebirs35391
HLIrs35391
Exacrs35391
Varsomers35391
Maprs35391
PheGenIrs35391
hapmaprs35391
1000 genomesrs35391
hgdprs35391
ensemblrs35391
gopubmedrs35391
geneviewrs35391
scholarrs35391
googlers35391
pharmgkbrs35391
gwascentralrs35391
openSNPrs35391
23andMers35391
23andMe allrs35391
SNP Nexus

SNPshotrs35391
SNPdbers35391
MSV3drs35391
GWAS Ctlgrs35391
GMAF0.3177
Max Magnitude0
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 19340012OA-icon.png]
Trait Tanning
Title Genome-Wide Association Study of Tanning Phenotype in a Population of European Ancestry
Risk Allele T
P-val 3E-10
Odds Ratio


[PMID 19710684OA-icon.png] Multiple pigmentation gene polymorphisms account for a substantial proportion of risk of cutaneous malignant melanoma

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


GET Evidence
rs35391
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.664062
summary