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rs28939697

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in complete genomics
Make rs28939697(C;C)
Make rs28939697(C;T)
ReferenceGRCh37 37.1/131
Chromosome16
Position60689551
GeneGNPATP
is asnp
is mentioned by
dbSNPrs28939697
ebirs28939697
HLIrs28939697
Exacrs28939697
Varsomers28939697
Maprs28939697
PheGenIrs28939697
hapmaprs28939697
1000 genomesrs28939697
hgdprs28939697
ensemblrs28939697
gopubmedrs28939697
geneviewrs28939697
scholarrs28939697
googlers28939697
pharmgkbrs28939697
gwascentralrs28939697
openSNPrs28939697
23andMers28939697
23andMe allrs28939697
SNP Nexus

SNPshotrs28939697
SNPdbers28939697
MSV3drs28939697
GWAS Ctlgrs28939697
StatusDeleted
Max Magnitude0
OMIM602744
DescRHIZOMELIC CHONDRODYSPLASIA PUNCTATA, TYPE 2
Variant0002
Relatedalso
Neighborrs28939696
Distance1