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rs6544997

From SNPedia

Orientationplus
Stabilizedplus
Make rs6544997(A;A)
Make rs6544997(A;G)
Make rs6544997(G;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position47617366
is asnp
is mentioned by
dbSNPrs6544997
ebirs6544997
HLIrs6544997
Exacrs6544997
Varsomers6544997
Maprs6544997
PheGenIrs6544997
hapmaprs6544997
1000 genomesrs6544997
hgdprs6544997
ensemblrs6544997
gopubmedrs6544997
geneviewrs6544997
scholarrs6544997
googlers6544997
pharmgkbrs6544997
gwascentralrs6544997
openSNPrs6544997
23andMers6544997
23andMe allrs6544997
SNP Nexus

SNPshotrs6544997
SNPdbers6544997
MSV3drs6544997
GWAS Ctlgrs6544997
GMAF0.45
Max Magnitude
? (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 0.000007
Odds Ratio NR NR


GET Evidence
rs6544997
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.609375
summary