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rs154659

From SNPedia

Orientationplus
Stabilizedplus
Make rs154659(C;C)
Make rs154659(C;T)
Make rs154659(T;T)
ReferenceGRCh38 38.1/141
Chromosome16
Position89600929
is asnp
is mentioned by
dbSNPrs154659
ebirs154659
HLIrs154659
Exacrs154659
Varsomers154659
Maprs154659
PheGenIrs154659
hapmaprs154659
1000 genomesrs154659
hgdprs154659
ensemblrs154659
gopubmedrs154659
geneviewrs154659
scholarrs154659
googlers154659
pharmgkbrs154659
gwascentralrs154659
openSNPrs154659
23andMers154659
23andMe allrs154659
SNP Nexus

SNPshotrs154659
SNPdbers154659
MSV3drs154659
GWAS Ctlgrs154659
GMAF0.36
Max Magnitude
? (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 C
P-val 7E-8
Odds Ratio


[PMID 18076761OA-icon.png] In silico and in vitro comparative analysis to select, validate and test SNPs for human identification.


[PMID 19366436OA-icon.png] Whole genome amplification and real-time PCR in forensic casework.


[PMID 20585627OA-icon.png] Web-based, participant-driven studies yield novel genetic associations for common traits.


GET Evidence
rs154659
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.375
summary