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rs6686842

From SNPedia

Orientationplus
Stabilizedplus
Make rs6686842(C;C)
Make rs6686842(C;T)
Make rs6686842(T;T)
ReferenceGRCh38 38.1/141
Chromosome1
Position41065199
GeneSCMH1
is asnp
is mentioned by
dbSNPrs6686842
ebirs6686842
HLIrs6686842
Exacrs6686842
Varsomers6686842
Maprs6686842
PheGenIrs6686842
hapmaprs6686842
1000 genomesrs6686842
hgdprs6686842
ensemblrs6686842
gopubmedrs6686842
geneviewrs6686842
scholarrs6686842
googlers6686842
pharmgkbrs6686842
gwascentralrs6686842
openSNPrs6686842
23andMers6686842
23andMe allrs6686842
SNP Nexus

SNPshotrs6686842
SNPdbers6686842
MSV3drs6686842
GWAS Ctlgrs6686842
GMAF0.3705
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 18391952OA-icon.png]
Trait Height
Title Genome-wide association analysis identifies 20 loci that influence adult height
Risk Allele C
P-val 2E-8
Odds Ratio 0.05 [0.02-0.08] SD shorter - among males

[PMID 19030899OA-icon.png] Genome-wide association scan for stature in Chinese: evidence for ethnic specific loci.

[PMID 19039035OA-icon.png] Genome-wide association study identifies two novel loci containing FLNB and SBF2 genes underlying stature variation.

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


GET Evidence
rs6686842
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.695312
summary