Have questions? Visit https://www.reddit.com/r/SNPedia

rs794726868

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs794726868(G;T)
Make rs794726868(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome12
Position20616306
GenePDE3A
is asnp
is mentioned by
dbSNPrs794726868
ebirs794726868
HLIrs794726868
Exacrs794726868
Varsomers794726868
Maprs794726868
PheGenIrs794726868
hapmaprs794726868
1000 genomesrs794726868
hgdprs794726868
ensemblrs794726868
gopubmedrs794726868
geneviewrs794726868
scholarrs794726868
googlers794726868
pharmgkbrs794726868
gwascentralrs794726868
openSNPrs794726868
23andMers794726868
23andMe allrs794726868
SNP Nexus

SNPshotrs794726868
SNPdbers794726868
MSV3drs794726868
GWAS Ctlgrs794726868
Max Magnitude0
ClinVar
Risk rs794726868(T;T)
Alt rs794726868(T;T)
Reference rs794726868(G;G)
Significance Pathogenic
Disease Brachydactyly with hypertension
Variation info
Gene PDE3A
CLNDBN Brachydactyly with hypertension
Reversed 0
HGVS NC_000012.11:g.20769240G>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000173043.2,