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rs10104997

From SNPedia

Orientationplus
Stabilizedplus
Make rs10104997(C;C)
Make rs10104997(C;T)
Make rs10104997(T;T)
ReferenceGRCh38 38.1/141
Chromosome8
Position54527508
is asnp
is mentioned by
dbSNPrs10104997
ebirs10104997
HLIrs10104997
Exacrs10104997
Varsomers10104997
Maprs10104997
PheGenIrs10104997
hapmaprs10104997
1000 genomesrs10104997
hgdprs10104997
ensemblrs10104997
gopubmedrs10104997
geneviewrs10104997
scholarrs10104997
googlers10104997
pharmgkbrs10104997
gwascentralrs10104997
openSNPrs10104997
23andMers10104997
23andMe allrs10104997
SNP Nexus

SNPshotrs10104997
SNPdbers10104997
MSV3drs10104997
GWAS Ctlgrs10104997
GMAF0.1892
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 22001756OA-icon.png]
Trait
Title Genome-wide association study identifies susceptibility loci for dengue shock syndrome at MICB and PLCE1.
Risk Allele
P-val 9E-7
Odds Ratio 1.2000 None