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rs797046098

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs797046098(A;A)
Make rs797046098(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome8
Position99820043
GeneVPS13B
is asnp
is mentioned by
dbSNPrs797046098
ebirs797046098
HLIrs797046098
Exacrs797046098
Varsomers797046098
Maprs797046098
PheGenIrs797046098
hapmaprs797046098
1000 genomesrs797046098
hgdprs797046098
ensemblrs797046098
gopubmedrs797046098
geneviewrs797046098
scholarrs797046098
googlers797046098
pharmgkbrs797046098
gwascentralrs797046098
openSNPrs797046098
23andMers797046098
23andMe allrs797046098
SNP Nexus

SNPshotrs797046098
SNPdbers797046098
MSV3drs797046098
GWAS Ctlgrs797046098
Max Magnitude0
ClinVar
Risk rs797046098(A;A)
Alt rs797046098(A;A)
Reference rs797046098(G;G)
Significance Pathogenic
Disease Cohen syndrome
Variation info
Gene VPS13B
CLNDBN Cohen syndrome
Reversed 0
HGVS NC_000008.10:g.100832271G>A
CLNSRC
CLNACC RCV000192341.1,