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rs1057520768

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057520768(A;A)
Make rs1057520768(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome8
Position99096311
GeneVPS13B
is asnp
is mentioned by
dbSNPrs1057520768
dbSNP (old)rs1057520768
ClinGenrs1057520768
ebirs1057520768
HLIrs1057520768
Exacrs1057520768
Gnomadrs1057520768
Varsomers1057520768
Maprs1057520768
PheGenIrs1057520768
Biobankrs1057520768
1000 genomesrs1057520768
hgdprs1057520768
ensemblrs1057520768
gopubmedrs1057520768
geneviewrs1057520768
scholarrs1057520768
googlers1057520768
pharmgkbrs1057520768
gwascentralrs1057520768
openSNPrs1057520768
23andMers1057520768
23andMe allrs1057520768
SNPshotrs1057520768
SNPdbers1057520768
MSV3drs1057520768
GWAS Ctlgrs1057520768
Max Magnitude0
ClinVar
Risk rs1057520768(A;A)
Alt rs1057520768(A;A)
Reference Rs1057520768(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene VPS13B
CLNDBN not provided
Reversed 0
HGVS NC_000008.10:g.100108539G>A
CLNSRC
CLNACC RCV000419213.1,