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rs2564921

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs2564921(A;G)
Make rs2564921(G;G)
ReferenceGRCh38 38.1/141
Chromosome3
Position53091569
GeneRFT1
is asnp
is mentioned by
dbSNPrs2564921
dbSNP (old)rs2564921
ClinGenrs2564921
ebirs2564921
HLIrs2564921
Exacrs2564921
Gnomadrs2564921
Varsomers2564921
Maprs2564921
PheGenIrs2564921
Biobankrs2564921
1000 genomesrs2564921
hgdprs2564921
ensemblrs2564921
gopubmedrs2564921
geneviewrs2564921
scholarrs2564921
googlers2564921
pharmgkbrs2564921
gwascentralrs2564921
openSNPrs2564921
23andMers2564921
23andMe allrs2564921
SNP Nexus

SNPshotrs2564921
SNPdbers2564921
MSV3drs2564921
GWAS Ctlgrs2564921
GMAF0.455
Max Magnitude0
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 23563607OA-icon.png]
Trait Height
Title Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture.
Risk Allele T
P-val 2E-12
Odds Ratio 1.15 [NR]


ClinVar
Risk rs2564921(G;G)
Alt rs2564921(G;G)
Reference Rs2564921(A;A)
Significance Non-pathogenic
Disease Congenital disorder of glycosylation
Variation info
Gene RFT1
CLNDBN Congenital disorder of glycosylation
Reversed 1
HGVS NC_000003.11:g.53125585T>C
CLNSRC
CLNACC RCV000365605.1,