rs1057519063

Orientation

minus

Stabilized

minus

Geno	Mag	Summary
(C;C)	0	common in clinvar

Make rs1057519063(C;T)

Make rs1057519063(T;T)

Reference

GRCh38.p7 38.3/150

Chromosome

15

Position

91013842

Gene	LOC105370970, VPS33B

is a	snp
is	mentioned by
dbSNP	rs1057519063
dbSNP (classic)	rs1057519063
ClinGen	rs1057519063
ebi	rs1057519063
HLI	rs1057519063
Exac	rs1057519063
Gnomad	rs1057519063
Varsome	rs1057519063
LitVar	rs1057519063
Map	rs1057519063
PheGenI	rs1057519063
Biobank	rs1057519063
1000 genomes	rs1057519063
hgdp	rs1057519063
ensembl	rs1057519063
geneview	rs1057519063
scholar	rs1057519063
google	rs1057519063
pharmgkb	rs1057519063
gwascentral	rs1057519063
openSNP	rs1057519063
23andMe	rs1057519063
SNPshot	rs1057519063
SNPdbe	rs1057519063
MSV3d	rs1057519063
GWAS Ctlg	rs1057519063

Max Magnitude

0

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,