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rs1016988

From SNPedia

Orientationplus
Stabilizedplus
Make rs1016988(C;C)
Make rs1016988(C;T)
Make rs1016988(T;T)
ReferenceGRCh38 38.1/141
Chromosome5
Position132408882
GeneC5orf56
is asnp
is mentioned by
dbSNPrs1016988
ebirs1016988
HLIrs1016988
Exacrs1016988
Varsomers1016988
Maprs1016988
PheGenIrs1016988
hapmaprs1016988
1000 genomesrs1016988
hgdprs1016988
ensemblrs1016988
gopubmedrs1016988
geneviewrs1016988
scholarrs1016988
googlers1016988
pharmgkbrs1016988
gwascentralrs1016988
openSNPrs1016988
23andMers1016988
23andMe allrs1016988
SNP Nexus

SNPshotrs1016988
SNPdbers1016988
MSV3drs1016988
GWAS Ctlgrs1016988
GMAF0.2029
Max Magnitude
? (C;C) (C;T) (T;T) 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 G
P-val 1E-12
Odds Ratio 6.84 [NR] mg/dl decrease


[PMID 20031576OA-icon.png] Association of novel genetic Loci with circulating fibrinogen levels: a genome-wide association study in 6 population-based cohorts.


GET Evidence
rs1016988
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.210938
summary