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rs2554380

From SNPedia

Orientationplus
Stabilizedplus
Make rs2554380(C;C)
Make rs2554380(C;T)
Make rs2554380(T;T)
ReferenceGRCh38 38.1/141
Chromosome15
Position83647132
is asnp
is mentioned by
dbSNPrs2554380
ebirs2554380
HLIrs2554380
Exacrs2554380
Varsomers2554380
Maprs2554380
PheGenIrs2554380
hapmaprs2554380
1000 genomesrs2554380
hgdprs2554380
ensemblrs2554380
gopubmedrs2554380
geneviewrs2554380
scholarrs2554380
googlers2554380
pharmgkbrs2554380
gwascentralrs2554380
openSNPrs2554380
23andMers2554380
23andMe allrs2554380
SNP Nexus

SNPshotrs2554380
SNPdbers2554380
MSV3drs2554380
GWAS Ctlgrs2554380
GMAF0.1102
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 T
P-val 8.9999999999999996E-7
Odds Ratio 4.50 [2.74-6.26] % 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
rs2554380
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.888889
summary