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rs6700896

From SNPedia

Orientationplus
Stabilizedplus
Make rs6700896(C;C)
Make rs6700896(C;T)
Make rs6700896(T;T)
ReferenceGRCh38 38.1/141
Chromosome1
Position65624099
GeneLEPR
is asnp
is mentioned by
dbSNPrs6700896
ebirs6700896
HLIrs6700896
Exacrs6700896
Varsomers6700896
Maprs6700896
PheGenIrs6700896
hapmaprs6700896
1000 genomesrs6700896
hgdprs6700896
ensemblrs6700896
gopubmedrs6700896
geneviewrs6700896
scholarrs6700896
googlers6700896
pharmgkbrs6700896
gwascentralrs6700896
openSNPrs6700896
23andMers6700896
23andMe allrs6700896
SNP Nexus

SNPshotrs6700896
SNPdbers6700896
MSV3drs6700896
GWAS Ctlgrs6700896
GMAF0.4591
Max Magnitude
? (C;C) (C;T) (T;T) 28
23andMe blog rs6700896(T) -14.8% lower CRP and associated with increased weight and body mass index


[PMID 19567438OA-icon.png] Genetic Loci associated with C-reactive protein levels and risk of coronary heart disease


[PMID 22215535] Association of nonalcoholic fatty liver disease with a single nucleotide polymorphism on the gene encoding leptin receptor


GET Evidence
rs6700896
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.441667
summary