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rs794726865

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs794726865(A;G)
Make rs794726865(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome12
Position20616293
GenePDE3A
is asnp
is mentioned by
dbSNPrs794726865
ebirs794726865
HLIrs794726865
Exacrs794726865
Varsomers794726865
Maprs794726865
PheGenIrs794726865
hapmaprs794726865
1000 genomesrs794726865
hgdprs794726865
ensemblrs794726865
gopubmedrs794726865
geneviewrs794726865
scholarrs794726865
googlers794726865
pharmgkbrs794726865
gwascentralrs794726865
openSNPrs794726865
23andMers794726865
23andMe allrs794726865
SNP Nexus

SNPshotrs794726865
SNPdbers794726865
MSV3drs794726865
GWAS Ctlgrs794726865
Max Magnitude0
ClinVar
Risk rs794726865(G;G)
Alt rs794726865(G;G)
Reference rs794726865(A;A)
Significance Pathogenic
Disease Brachydactyly with hypertension
Variation info
Gene PDE3A
CLNDBN Brachydactyly with hypertension
Reversed 0
HGVS NC_000012.11:g.20769227A>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000173039.2,