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rs535043

From SNPedia

Orientationminus
Stabilizedminus
Make rs535043(C;C)
Make rs535043(C;T)
Make rs535043(T;T)
ReferenceGRCh38 38.1/141
Chromosome1
Position238532736
is asnp
is mentioned by
dbSNPrs535043
ebirs535043
HLIrs535043
Exacrs535043
Varsomers535043
Maprs535043
PheGenIrs535043
hapmaprs535043
1000 genomesrs535043
hgdprs535043
ensemblrs535043
gopubmedrs535043
geneviewrs535043
scholarrs535043
googlers535043
pharmgkbrs535043
gwascentralrs535043
openSNPrs535043
23andMers535043
23andMe allrs535043
SNP Nexus

SNPshotrs535043
SNPdbers535043
MSV3drs535043
GWAS Ctlgrs535043
GMAF0.3333
Max Magnitude
? (C;C) (C;T) (T;T) 28
OMIM119100
DescSPLIT-HAND/FOOT MALFORMATION WITH LONG BONE DEFICIENCY 1; SHFLD1
Variant
Relatedalso
[PMID 17160898OA-icon.png] Genomewide linkage scan for split-hand/foot malformation with long-bone deficiency in a large Arab family identifies two novel susceptibility loci on chromosomes 1q42.2-q43 and 6q14.1.


[PMID 17903300OA-icon.png] Genome-wide association to body mass index and waist circumference: the Framingham Heart Study 100K project.