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rs2110001

From SNPedia

Orientationminus
Stabilizedminus
Make rs2110001(C;C)
Make rs2110001(C;G)
Make rs2110001(G;G)
ReferenceGRCh38 38.1/141
Chromosome7
Position150819934
is asnp
is mentioned by
dbSNPrs2110001
ebirs2110001
HLIrs2110001
Exacrs2110001
Varsomers2110001
Maprs2110001
PheGenIrs2110001
hapmaprs2110001
1000 genomesrs2110001
hgdprs2110001
ensemblrs2110001
gopubmedrs2110001
geneviewrs2110001
scholarrs2110001
googlers2110001
pharmgkbrs2110001
gwascentralrs2110001
openSNPrs2110001
23andMers2110001
23andMe allrs2110001
SNP Nexus

SNPshotrs2110001
SNPdbers2110001
MSV3drs2110001
GWAS Ctlgrs2110001
GMAF0.4642
Max Magnitude
? (C;C) (C;G) (G;G) 28
GWAS snp
PMID [PMID 20881960OA-icon.png]
Trait Height
Title Hundreds of variants clustered in genomic loci and biological pathways affect human height.
Risk Allele C
P-val 3E-13
Odds Ratio .03 [NR] unit decrease