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rs31198

From SNPedia

Orientationplus
Stabilizedplus
Make rs31198(C;C)
Make rs31198(C;T)
Make rs31198(T;T)
ReferenceGRCh38 38.1/141
Chromosome5
Position135036995
GeneC5orf66
is asnp
is mentioned by
dbSNPrs31198
ebirs31198
HLIrs31198
Exacrs31198
Varsomers31198
Maprs31198
PheGenIrs31198
hapmaprs31198
1000 genomesrs31198
hgdprs31198
ensemblrs31198
gopubmedrs31198
geneviewrs31198
scholarrs31198
googlers31198
pharmgkbrs31198
gwascentralrs31198
openSNPrs31198
23andMers31198
23andMe allrs31198
SNP Nexus

SNPshotrs31198
SNPdbers31198
MSV3drs31198
GWAS Ctlgrs31198
GMAF0.3219
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 0.0000079999999999999996
Odds Ratio 4.80 [2.64-6.96] % SD taller


[PMID 20017971OA-icon.png] Assessing the impact of global versus local ancestry in association studies.


GET Evidence
rs31198
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.226562
summary