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rs794726666

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs794726666(-;-)
Make rs794726666(-;G)
ReferenceGRCh38.p2 38.2/146
Chromosome4
Position5804737
GeneEVC
is asnp
is mentioned by
dbSNPrs794726666
ebirs794726666
HLIrs794726666
Exacrs794726666
Varsomers794726666
Maprs794726666
PheGenIrs794726666
hapmaprs794726666
1000 genomesrs794726666
hgdprs794726666
ensemblrs794726666
gopubmedrs794726666
geneviewrs794726666
scholarrs794726666
googlers794726666
pharmgkbrs794726666
gwascentralrs794726666
openSNPrs794726666
23andMers794726666
23andMe allrs794726666
SNP Nexus

SNPshotrs794726666
SNPdbers794726666
MSV3drs794726666
GWAS Ctlgrs794726666
Max Magnitude0
ClinVar
Risk rs794726666(;)
Alt rs794726666(;)
Reference rs794726666(G;G)
Significance Pathogenic
Disease Chondroectodermal dysplasia
Variation info
Gene EVC
CLNDBN Chondroectodermal dysplasia
Reversed 0
HGVS NC_000004.11:g.5806464delG
CLNSRC OMIM Allelic Variant
CLNACC RCV000005673.4,