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rs1057519063

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1057519063(C;T)
Make rs1057519063(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome15
Position91013842
GeneLOC105370970, VPS33B
is asnp
is mentioned by
dbSNPrs1057519063
dbSNP (old)rs1057519063
ClinGenrs1057519063
ebirs1057519063
HLIrs1057519063
Exacrs1057519063
Gnomadrs1057519063
Varsomers1057519063
Maprs1057519063
PheGenIrs1057519063
Biobankrs1057519063
1000 genomesrs1057519063
hgdprs1057519063
ensemblrs1057519063
gopubmedrs1057519063
geneviewrs1057519063
scholarrs1057519063
googlers1057519063
pharmgkbrs1057519063
gwascentralrs1057519063
openSNPrs1057519063
23andMers1057519063
23andMe allrs1057519063
SNPshotrs1057519063
SNPdbers1057519063
MSV3drs1057519063
GWAS Ctlgrs1057519063
Max Magnitude0
ClinVar
Risk rs1057519063(T;T)
Alt rs1057519063(T;T)
Reference Rs1057519063(C;C)
Significance Pathogenic
Disease Arthrogryposis renal dysfunction cholestasis syndrome
Variation info
Gene VPS33B
CLNDBN Arthrogryposis renal dysfunction cholestasis syndrome
Reversed 1
HGVS NC_000015.9:g.91557072G>A
CLNSRC
CLNACC RCV000416361.1,