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rs955748

From SNPedia

Orientationminus
Stabilizedminus
Make rs955748(C;C)
Make rs955748(C;T)
Make rs955748(T;T)
ReferenceGRCh38 38.1/141
Chromosome4
Position183294522
GeneWWC2
is asnp
is mentioned by
dbSNPrs955748
ebirs955748
HLIrs955748
Exacrs955748
Varsomers955748
Maprs955748
PheGenIrs955748
hapmaprs955748
1000 genomesrs955748
hgdprs955748
ensemblrs955748
gopubmedrs955748
geneviewrs955748
scholarrs955748
googlers955748
pharmgkbrs955748
gwascentralrs955748
openSNPrs955748
23andMers955748
23andMe allrs955748
SNP Nexus

SNPshotrs955748
SNPdbers955748
MSV3drs955748
GWAS Ctlgrs955748
GMAF0.3627
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 20881960OA-icon.png]
Trait Height
Title Hundreds of variants clustered in genomic loci and biological pathways affect human height.
Risk Allele A
P-val 4E-8
Odds Ratio .02 [NR] unit decrease


[PMID 19343178OA-icon.png] Meta-analysis of genome-wide scans for human adult stature identifies novel Loci and associations with measures of skeletal frame size.