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rs7703051

From SNPedia

Orientationplus
Stabilizedplus
Make rs7703051(A;A)
Make rs7703051(A;C)
Make rs7703051(C;C)
ReferenceGRCh38 38.1/141
Chromosome5
Position75329662
is asnp
is mentioned by
dbSNPrs7703051
ebirs7703051
HLIrs7703051
Exacrs7703051
Varsomers7703051
Maprs7703051
PheGenIrs7703051
hapmaprs7703051
1000 genomesrs7703051
hgdprs7703051
ensemblrs7703051
gopubmedrs7703051
geneviewrs7703051
scholarrs7703051
googlers7703051
pharmgkbrs7703051
gwascentralrs7703051
openSNPrs7703051
23andMers7703051
23andMe allrs7703051
SNP Nexus

SNPshotrs7703051
SNPdbers7703051
MSV3drs7703051
GWAS Ctlgrs7703051
GMAF0.4201
Max Magnitude
? (A;A) (A;C) (C;C) 28
GWAS snp
PMID [PMID 18802019OA-icon.png]
Trait LDL cholesterol
Title Common SNPs in HMGCR in Micronesians and Whites Associated With LDL-Cholesterol Levels Affect Alternative Splicing of Exon13
Risk Allele A
P-val 1E-8
Odds Ratio 18.00 [NR] % SD increase



GET Evidence
rs7703051
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.398438
summary