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rs794726867

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs794726867(C;T)
Make rs794726867(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome12
Position20616300
GenePDE3A
is asnp
is mentioned by
dbSNPrs794726867
ebirs794726867
HLIrs794726867
Exacrs794726867
Varsomers794726867
Maprs794726867
PheGenIrs794726867
hapmaprs794726867
1000 genomesrs794726867
hgdprs794726867
ensemblrs794726867
gopubmedrs794726867
geneviewrs794726867
scholarrs794726867
googlers794726867
pharmgkbrs794726867
gwascentralrs794726867
openSNPrs794726867
23andMers794726867
23andMe allrs794726867
SNP Nexus

SNPshotrs794726867
SNPdbers794726867
MSV3drs794726867
GWAS Ctlgrs794726867
Max Magnitude0
ClinVar
Risk rs794726867(T;T)
Alt rs794726867(T;T)
Reference rs794726867(C;C)
Significance Pathogenic
Disease Brachydactyly with hypertension
Variation info
Gene PDE3A
CLNDBN Brachydactyly with hypertension
Reversed 0
HGVS NC_000012.11:g.20769234C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000173042.2,