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rs1668873

From SNPedia

Orientationminus
Stabilizedminus
Make rs1668873(C;C)
Make rs1668873(C;T)
Make rs1668873(T;T)
ReferenceGRCh38 38.1/141
Chromosome1
Position205266862
GeneLOC100506871, TMCC2
is asnp
is mentioned by
dbSNPrs1668873
ebirs1668873
HLIrs1668873
Exacrs1668873
Varsomers1668873
Maprs1668873
PheGenIrs1668873
hapmaprs1668873
1000 genomesrs1668873
hgdprs1668873
ensemblrs1668873
gopubmedrs1668873
geneviewrs1668873
scholarrs1668873
googlers1668873
pharmgkbrs1668873
gwascentralrs1668873
openSNPrs1668873
23andMers1668873
23andMe allrs1668873
SNP Nexus

SNPshotrs1668873
SNPdbers1668873
MSV3drs1668873
GWAS Ctlgrs1668873
GMAF0.1942
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 19820697OA-icon.png]
Trait MPV
Title A genome-wide meta-analysis identifies 22 loci associated with eight hematological parameters in the HaemGen consortium
Risk Allele G
P-val 1E-20
Odds Ratio 0.01 [0.01-0.014] fl increase


GET Evidence
rs1668873
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.25
summary