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rs781781537

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs781781537(C;T)
Make rs781781537(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome8
Position99442587
GeneVPS13B
is asnp
is mentioned by
dbSNPrs781781537
ebirs781781537
HLIrs781781537
Exacrs781781537
Varsomers781781537
Maprs781781537
PheGenIrs781781537
hapmaprs781781537
1000 genomesrs781781537
hgdprs781781537
ensemblrs781781537
gopubmedrs781781537
geneviewrs781781537
scholarrs781781537
googlers781781537
pharmgkbrs781781537
gwascentralrs781781537
openSNPrs781781537
23andMers781781537
23andMe allrs781781537
SNP Nexus

SNPshotrs781781537
SNPdbers781781537
MSV3drs781781537
GWAS Ctlgrs781781537
Max Magnitude0
ClinVar
Risk rs781781537(A,T;A,T)
Alt rs781781537(A,T;A,T)
Reference rs781781537(C;C)
Significance Probable-Pathogenic
Disease Inborn genetic diseases
Variation info
Gene VPS13B
CLNDBN Inborn genetic diseases
Reversed 0
HGVS NC_000008.10:g.100454815C>T
CLNSRC
CLNACC RCV000210717.1,