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rs3825199

From SNPedia

Orientationminus
Stabilizedminus
Make rs3825199(C;C)
Make rs3825199(C;T)
Make rs3825199(T;T)
ReferenceGRCh38 38.1/141
Chromosome12
Position93583178
GeneSOCS2
is asnp
is mentioned by
dbSNPrs3825199
ebirs3825199
HLIrs3825199
Exacrs3825199
Varsomers3825199
Maprs3825199
PheGenIrs3825199
hapmaprs3825199
1000 genomesrs3825199
hgdprs3825199
ensemblrs3825199
gopubmedrs3825199
geneviewrs3825199
scholarrs3825199
googlers3825199
pharmgkbrs3825199
gwascentralrs3825199
openSNPrs3825199
23andMers3825199
23andMe allrs3825199
SNP Nexus

SNPshotrs3825199
SNPdbers3825199
MSV3drs3825199
GWAS Ctlgrs3825199
GMAF0.2608
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 18391951]
Trait Height
Title Many sequence variants affecting diversity of adult human height
Risk Allele C
P-val 1.9999999999999999E-7
Odds Ratio 6.20 [3.85-8.55] % SD taller


[PMID 20546612OA-icon.png] The role of height-associated loci identified in genome wide association studies in the determination of pediatric stature.


GET Evidence
rs3825199
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.18254
summary