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rs6750795

From SNPedia

Orientationplus
Stabilizedplus
Make rs6750795(C;C)
Make rs6750795(C;T)
Make rs6750795(T;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position231513520
GeneLINC00471
is asnp
is mentioned by
dbSNPrs6750795
dbSNP (classic)rs6750795
ClinGenrs6750795
ebirs6750795
HLIrs6750795
Exacrs6750795
Gnomadrs6750795
Varsomers6750795
LitVarrs6750795
Maprs6750795
PheGenIrs6750795
Biobankrs6750795
1000 genomesrs6750795
hgdprs6750795
ensemblrs6750795
geneviewrs6750795
scholarrs6750795
googlers6750795
pharmgkbrs6750795
gwascentralrs6750795
openSNPrs6750795
23andMers6750795
SNPshotrs6750795
SNPdbers6750795
MSV3drs6750795
GWAS Ctlgrs6750795
GMAF0.4229
Max Magnitude0
? (C;C) (C;T) (T;T) 28


GWAS snp
PMID [PMID 23563607OA-icon.png]
Trait Height
Title Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture.
Risk Allele T
P-val 2E-8
Odds Ratio 1.12 [NR]