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rs869312923

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs869312923(C;T)
Make rs869312923(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome8
Position99192952
GeneVPS13B
is asnp
is mentioned by
dbSNPrs869312923
ebirs869312923
HLIrs869312923
Exacrs869312923
Varsomers869312923
Maprs869312923
PheGenIrs869312923
hapmaprs869312923
1000 genomesrs869312923
hgdprs869312923
ensemblrs869312923
gopubmedrs869312923
geneviewrs869312923
scholarrs869312923
googlers869312923
pharmgkbrs869312923
gwascentralrs869312923
openSNPrs869312923
23andMers869312923
23andMe allrs869312923
SNP Nexus

SNPshotrs869312923
SNPdbers869312923
MSV3drs869312923
GWAS Ctlgrs869312923
Max Magnitude0
ClinVar
Risk rs869312923(T;T)
Alt rs869312923(T;T)
Reference rs869312923(C;C)
Significance Pathogenic
Disease Inborn genetic diseases
Variation info
Gene VPS13B
CLNDBN Inborn genetic diseases
Reversed 0
HGVS NC_000008.10:g.100205180C>T
CLNSRC
CLNACC RCV000210577.1,