rs1057520769

Orientation

plus

Stabilized

plus

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

Make rs1057520769(A;T)

Make rs1057520769(T;T)

Reference

GRCh38.p7 38.3/150

Chromosome

8

Position

99854124

Gene

VPS13B

is a	snp
is	mentioned by
dbSNP	rs1057520769
dbSNP (classic)	rs1057520769
ClinGen	rs1057520769
ebi	rs1057520769
HLI	rs1057520769
Exac	rs1057520769
Gnomad	rs1057520769
Varsome	rs1057520769
LitVar	rs1057520769
Map	rs1057520769
PheGenI	rs1057520769
Biobank	rs1057520769
1000 genomes	rs1057520769
hgdp	rs1057520769
ensembl	rs1057520769
geneview	rs1057520769
scholar	rs1057520769
google	rs1057520769
pharmgkb	rs1057520769
gwascentral	rs1057520769
openSNP	rs1057520769
23andMe	rs1057520769
SNPshot	rs1057520769
SNPdbe	rs1057520769
MSV3d	rs1057520769
GWAS Ctlg	rs1057520769

Max Magnitude

0

ClinVar
Risk	rs1057520769(T;T)
Alt	rs1057520769(T;T)
Reference	Rs1057520769(A;A)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	VPS13B
CLNDBN	not provided
Reversed	0
HGVS	NC_000008.10:g.100866352A>T
CLNSRC
CLNACC	RCV000429941.1,