rs1057519182

Orientation

plus

Stabilized

plus

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

Make rs1057519182(G;G)

Make rs1057519182(G;T)

Reference

GRCh38.p7 38.3/150

Chromosome

8

Position

99121241

Gene

VPS13B

is a	snp
is	mentioned by
dbSNP	rs1057519182
dbSNP (classic)	rs1057519182
ClinGen	rs1057519182
ebi	rs1057519182
HLI	rs1057519182
Exac	rs1057519182
Gnomad	rs1057519182
Varsome	rs1057519182
LitVar	rs1057519182
Map	rs1057519182
PheGenI	rs1057519182
Biobank	rs1057519182
1000 genomes	rs1057519182
hgdp	rs1057519182
ensembl	rs1057519182
geneview	rs1057519182
scholar	rs1057519182
google	rs1057519182
pharmgkb	rs1057519182
gwascentral	rs1057519182
openSNP	rs1057519182
23andMe	rs1057519182
SNPshot	rs1057519182
SNPdbe	rs1057519182
MSV3d	rs1057519182
GWAS Ctlg	rs1057519182

Max Magnitude

0

ClinVar
Risk	rs1057519182(G;G)
Alt	rs1057519182(G;G)
Reference	Rs1057519182(T;T)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	VPS13B
CLNDBN	not provided
Reversed	0
HGVS	NC_000008.10:g.100133469T>G
CLNSRC
CLNACC	RCV000416267.2,