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rs2326458

From SNPedia

Orientationplus
Stabilizedplus
Make rs2326458(A;A)
Make rs2326458(A;C)
Make rs2326458(C;C)
ReferenceGRCh38 38.1/141
Chromosome16
Position84954073
is asnp
is mentioned by
dbSNPrs2326458
ebirs2326458
HLIrs2326458
Exacrs2326458
Varsomers2326458
Maprs2326458
PheGenIrs2326458
hapmaprs2326458
1000 genomesrs2326458
hgdprs2326458
ensemblrs2326458
gopubmedrs2326458
geneviewrs2326458
scholarrs2326458
googlers2326458
pharmgkbrs2326458
gwascentralrs2326458
openSNPrs2326458
23andMers2326458
23andMe allrs2326458
SNP Nexus

SNPshotrs2326458
SNPdbers2326458
MSV3drs2326458
GWAS Ctlgrs2326458
GMAF0.3255
Max Magnitude
? (A;A) (A;C) (C;C) 28
GWAS snp
PMID [PMID 18391951]
Trait Height
Title Many sequence variants affecting diversity of adult human height
Risk Allele C
P-val 7.9999999999999996E-7
Odds Ratio 5.10 [3.14-7.06] % SD taller
OMIM613547
Desc
Variant
Relatedalso


GET Evidence
rs2326458
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.671875
summary