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rs2833607

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0
Make rs2833607(A;A)
Make rs2833607(A;G)
ReferenceGRCh38 38.1/141
Chromosome21
Position32008727
is asnp
is mentioned by
dbSNPrs2833607
ebirs2833607
HLIrs2833607
Exacrs2833607
Varsomers2833607
Maprs2833607
PheGenIrs2833607
hapmaprs2833607
1000 genomesrs2833607
hgdprs2833607
ensemblrs2833607
gopubmedrs2833607
geneviewrs2833607
scholarrs2833607
googlers2833607
pharmgkbrs2833607
gwascentralrs2833607
openSNPrs2833607
23andMers2833607
23andMe allrs2833607
SNP Nexus

SNPshotrs2833607
SNPdbers2833607
MSV3drs2833607
GWAS Ctlgrs2833607
GMAF0.1864
Max Magnitude0
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 19890347OA-icon.png]
Trait Vitiligo
Title Genome-Wide Association Study of Generalized Vitiligo in an Isolated European Founder Population Identifies SMOC2, in Close Proximity to IDDM8
Risk Allele
P-val 0.000002
Odds Ratio NR NR


GET Evidence
rs2833607
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.15625
summary