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rs710841

From SNPedia

Orientationminus
Stabilizedplus
Make rs710841(A;A)
Make rs710841(A;G)
Make rs710841(G;G)
ReferenceGRCh38 38.1/142
Chromosome4
Position81228677
is asnp
is mentioned by
dbSNPrs710841
ebirs710841
HLIrs710841
Exacrs710841
Varsomers710841
Maprs710841
PheGenIrs710841
hapmaprs710841
1000 genomesrs710841
hgdprs710841
ensemblrs710841
gopubmedrs710841
geneviewrs710841
scholarrs710841
googlers710841
pharmgkbrs710841
gwascentralrs710841
openSNPrs710841
23andMers710841
23andMe allrs710841
SNP Nexus

SNPshotrs710841
SNPdbers710841
MSV3drs710841
GWAS Ctlgrs710841
GMAF0.3361
Max Magnitude
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 19343178OA-icon.png]
Trait Height
Title Meta-analysis of genome-wide scans for human adult stature identifies novel Loci and associations with measures of skeletal frame size
Risk Allele
P-val 2E-8
Odds Ratio
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 5.00 [3.04-6.96] % SD taller



GET Evidence
rs710841
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.420635
summary