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rs1064793747

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(CA;CA) 0 common in clinvar
Chromosome8
Position99861855
GeneVPS13B
is asnp
is mentioned by
dbSNPrs1064793747
dbSNP (old)rs1064793747
ClinGenrs1064793747
ebirs1064793747
HLIrs1064793747
Exacrs1064793747
Gnomadrs1064793747
Varsomers1064793747
LitVarrs1064793747
Maprs1064793747
PheGenIrs1064793747
Biobankrs1064793747
1000 genomesrs1064793747
hgdprs1064793747
ensemblrs1064793747
gopubmedrs1064793747
geneviewrs1064793747
scholarrs1064793747
googlers1064793747
pharmgkbrs1064793747
gwascentralrs1064793747
openSNPrs1064793747
23andMers1064793747
23andMe allrs1064793747
SNPshotrs1064793747
SNPdbers1064793747
MSV3drs1064793747
GWAS Ctlgrs1064793747
Max Magnitude0
ClinVar
Risk rs1064793747(T;T)
Alt rs1064793747(T;T)
Reference Rs1064793747(CA;CA)
Significance Pathogenic
Disease not provided
Variation info
Gene VPS13B
CLNDBN not provided
Reversed 0
HGVS NC_000008.10:g.100874083_100874084delCAinsT
CLNSRC
CLNACC RCV000483748.1,