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rs479777

From SNPedia

Orientationplus
Stabilizedplus
Make rs479777(C;C)
Make rs479777(C;T)
Make rs479777(T;T)
ReferenceGRCh38 38.1/141
Chromosome11
Position64340005
GeneCCDC88B, LOC102723878
is asnp
is mentioned by
dbSNPrs479777
dbSNP (classic)rs479777
ClinGenrs479777
ebirs479777
HLIrs479777
Exacrs479777
Gnomadrs479777
Varsomers479777
LitVarrs479777
Maprs479777
PheGenIrs479777
Biobankrs479777
1000 genomesrs479777
hgdprs479777
ensemblrs479777
geneviewrs479777
scholarrs479777
googlers479777
pharmgkbrs479777
gwascentralrs479777
openSNPrs479777
23andMers479777
SNPshotrs479777
SNPdbers479777
MSV3drs479777
GWAS Ctlgrs479777
GMAF0.2507
Max Magnitude0
? (C;C) (C;T) (T;T) 28


GWAS snp
PMID [PMID 22837380]
Trait Sarcoidosis
Title A novel sarcoidosis risk locus for Europeans on chromosome 11q13.1.
Risk Allele
P-val 3E-18
Odds Ratio 1.18 [1.18-1.43]