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rs7885458

From SNPedia

Orientationplus
Stabilizedplus
Make rs7885458(C;C)
Make rs7885458(C;T)
Make rs7885458(T;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position6302433
is asnp
is mentioned by
dbSNPrs7885458
ebirs7885458
HLIrs7885458
Exacrs7885458
Varsomers7885458
Maprs7885458
PheGenIrs7885458
hapmaprs7885458
1000 genomesrs7885458
hgdprs7885458
ensemblrs7885458
gopubmedrs7885458
geneviewrs7885458
scholarrs7885458
googlers7885458
pharmgkbrs7885458
gwascentralrs7885458
openSNPrs7885458
23andMers7885458
23andMe allrs7885458
SNP Nexus

SNPshotrs7885458
SNPdbers7885458
MSV3drs7885458
GWAS Ctlgrs7885458
GMAF0.2781
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 19260141OA-icon.png]
Trait Biochemical measures
Title Genome-wide association study of biochemical traits in Korcula Island, Croatia
Risk Allele G
P-val 0.000003
Odds Ratio 0.23 [0.13-0.33] g/L decrease
[PMID 19260141OA-icon.png] gwas among adults residing on Korcula Island in Croatia, fibrinogen, the G allele associated with decreased fibrinogen levels



GET Evidence
rs7885458
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.26087
summary