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rs10007186

From SNPedia

Orientationplus
Stabilizedplus
Make rs10007186(C;C)
Make rs10007186(C;T)
Make rs10007186(T;T)
ReferenceGRCh38 38.1/141
Chromosome4
Position78667891
GeneLINC00230A
is asnp
is mentioned by
dbSNPrs10007186
ebirs10007186
HLIrs10007186
Exacrs10007186
Varsomers10007186
Maprs10007186
PheGenIrs10007186
hapmaprs10007186
1000 genomesrs10007186
hgdprs10007186
ensemblrs10007186
gopubmedrs10007186
geneviewrs10007186
scholarrs10007186
googlers10007186
pharmgkbrs10007186
gwascentralrs10007186
openSNPrs10007186
23andMers10007186
23andMe allrs10007186
SNP Nexus

SNPshotrs10007186
SNPdbers10007186
MSV3drs10007186
GWAS Ctlgrs10007186
GMAF0.3664
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 22558069OA-icon.png]
Trait
Title Association of common variants in TNFRSF13B, TNFSF13, and ANXA3 with serum levels of non-albumin protein and immunoglobulin isotypes in Japanese.
Risk Allele C
P-val 1E-9
Odds Ratio 0.0850 None