Have questions? Visit https://www.reddit.com/r/SNPedia

rs10512597

From SNPedia

Orientationplus
Stabilizedplus
Make rs10512597(C;C)
Make rs10512597(C;T)
Make rs10512597(T;T)
ReferenceGRCh38 38.1/141
Chromosome17
Position74703694
GeneCD300LF, RAB37
is asnp
is mentioned by
dbSNPrs10512597
ebirs10512597
HLIrs10512597
Exacrs10512597
Varsomers10512597
Maprs10512597
PheGenIrs10512597
hapmaprs10512597
1000 genomesrs10512597
hgdprs10512597
ensemblrs10512597
gopubmedrs10512597
geneviewrs10512597
scholarrs10512597
googlers10512597
pharmgkbrs10512597
gwascentralrs10512597
openSNPrs10512597
23andMers10512597
23andMe allrs10512597
SNP Nexus

SNPshotrs10512597
SNPdbers10512597
MSV3drs10512597
GWAS Ctlgrs10512597
GMAF0.3554
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 A
P-val 8E-11
Odds Ratio 6.45 [NR] mg/dl decrease


GET Evidence
rs10512597
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.609375
summary



GWAS snp
PMID [PMID 23969696OA-icon.png]
Trait Fibrinogen
Title Multiethnic meta-analysis of genome-wide association studies in >100 000 subjects identifies 23 fibrinogen-associated Loci but no strong evidence of a causal association between circulating fibrinogen and cardiovascular disease.
Risk Allele T
P-val 1E-8
Odds Ratio .01 [0.006-0.01] unit decrease