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rs1064796925

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(TT;TT) 0 common in clinvar
Chromosome8
Position99699787
GeneVPS13B
is asnp
is mentioned by
dbSNPrs1064796925
dbSNP (old)rs1064796925
ClinGenrs1064796925
ebirs1064796925
HLIrs1064796925
Exacrs1064796925
Gnomadrs1064796925
Varsomers1064796925
LitVarrs1064796925
Maprs1064796925
PheGenIrs1064796925
Biobankrs1064796925
1000 genomesrs1064796925
hgdprs1064796925
ensemblrs1064796925
gopubmedrs1064796925
geneviewrs1064796925
scholarrs1064796925
googlers1064796925
pharmgkbrs1064796925
gwascentralrs1064796925
openSNPrs1064796925
23andMers1064796925
23andMe allrs1064796925
SNPshotrs1064796925
SNPdbers1064796925
MSV3drs1064796925
GWAS Ctlgrs1064796925
Max Magnitude0
ClinVar
Risk rs1064796925(-;-)
Alt rs1064796925(-;-)
Reference Rs1064796925(TT;TT)
Significance Pathogenic
Disease not provided
Variation info
Gene VPS13B
CLNDBN not provided
Reversed 0
HGVS NC_000008.10:g.100712015_100712016delTT
CLNSRC
CLNACC RCV000479240.1,