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rs2187642

From SNPedia

Orientationplus
Stabilizedplus
Make rs2187642(A;A)
Make rs2187642(A;C)
Make rs2187642(C;C)
ReferenceGRCh38 38.1/141
Chromosome12
Position11702690
GeneETV6
is asnp
is mentioned by
dbSNPrs2187642
ebirs2187642
HLIrs2187642
Exacrs2187642
Varsomers2187642
Maprs2187642
PheGenIrs2187642
hapmaprs2187642
1000 genomesrs2187642
hgdprs2187642
ensemblrs2187642
gopubmedrs2187642
geneviewrs2187642
scholarrs2187642
googlers2187642
pharmgkbrs2187642
gwascentralrs2187642
openSNPrs2187642
23andMers2187642
23andMe allrs2187642
SNP Nexus

SNPshotrs2187642
SNPdbers2187642
MSV3drs2187642
GWAS Ctlgrs2187642
GMAF0.4757
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 A
P-val 0.0000019999999999999999
Odds Ratio 4.60 [2.64-6.56] % SD taller


GET Evidence
rs2187642
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.460938
summary