Rs10479002

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Merged intors12777
Orientationplus
Make rs10479002(C;C)
Make rs10479002(C;G)
Make rs10479002(G;G)
ReferenceGRCh38 38.1/141
Chromosome5
Position132335969
GeneMIR4750, SLC22A4
is asnp
is mentioned by
dbSNPrs10479002
PheGenIrs10479002
nextbiors10479002
hapmaprs10479002
1000 genomesrs10479002
hgdprs10479002
ensemblrs10479002
gopubmedrs10479002
geneviewrs10479002
scholarrs10479002
googlers10479002
pharmgkbrs10479002
gwascentralrs10479002
openSNPrs10479002
23andMers10479002
23andMe allrs10479002
SNP Nexus

SNPshotrs10479002
SNPdbers10479002
MSV3drs10479002
StatusMerged into rs12777
Max Magnitude
? (C;C) (C;G) (G;G) 28
GWAS snp
PMID [PMID 20031577OA-icon.png]
Trait Fibrinogen
Title Novel Loci, Including Those Related to Crohn Disease, Psoriasis, and Inflammation Identified in a Genome-Wide Association Study of Fibrinogen in 17,686 Women: The Women's Genome Health Study
Risk Allele C
P-val 0.000001
Odds Ratio 9.51 [NR] mg/dl increase