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rs1085307957

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Chromosome8
Position99641950
GeneVPS13B
is asnp
is mentioned by
dbSNPrs1085307957
dbSNP (old)rs1085307957
ClinGenrs1085307957
ebirs1085307957
HLIrs1085307957
Exacrs1085307957
Gnomadrs1085307957
Varsomers1085307957
Maprs1085307957
PheGenIrs1085307957
Biobankrs1085307957
1000 genomesrs1085307957
hgdprs1085307957
ensemblrs1085307957
gopubmedrs1085307957
geneviewrs1085307957
scholarrs1085307957
googlers1085307957
pharmgkbrs1085307957
gwascentralrs1085307957
openSNPrs1085307957
23andMers1085307957
23andMe allrs1085307957
SNPshotrs1085307957
SNPdbers1085307957
MSV3drs1085307957
GWAS Ctlgrs1085307957
Max Magnitude0
ClinVar
Risk rs1085307957(T;T)
Alt rs1085307957(T;T)
Reference Rs1085307957(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene VPS13B
CLNDBN not provided
Reversed 0
HGVS NC_000008.10:g.100654178G>T
CLNSRC
CLNACC RCV000489122.1,