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rs794726653

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(CAGAA;CAGAA) 0 common in clinvar
Make rs794726653(-;-)
Make rs794726653(-;CAGAA)
ReferenceGRCh38.p2 38.2/146
Chromosome14
Position77441075
GeneVIPAS39
is asnp
is mentioned by
dbSNPrs794726653
dbSNP (old)rs794726653
ClinGenrs794726653
ebirs794726653
HLIrs794726653
Exacrs794726653
Gnomadrs794726653
Varsomers794726653
Maprs794726653
PheGenIrs794726653
Biobankrs794726653
1000 genomesrs794726653
hgdprs794726653
ensemblrs794726653
gopubmedrs794726653
geneviewrs794726653
scholarrs794726653
googlers794726653
pharmgkbrs794726653
gwascentralrs794726653
openSNPrs794726653
23andMers794726653
23andMe allrs794726653
SNP Nexus

SNPshotrs794726653
SNPdbers794726653
MSV3drs794726653
GWAS Ctlgrs794726653
Max Magnitude0
ClinVar
Risk rs794726653(-;-)
Alt rs794726653(-;-)
Reference Rs794726653(CAGAA;CAGAA)
Significance Pathogenic
Disease Arthrogryposis
Variation info
Gene VIPAS39
CLNDBN Arthrogryposis, renal dysfunction, and cholestasis 2
Reversed 1
HGVS NC_000014.8:g.77907418_77907422delTTCTG
CLNSRC OMIM Allelic Variant
CLNACC RCV000000132.5,