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rs753770252

From SNPedia

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Geno Mag Summary
(C;C) 0 common in clinvar
Make rs753770252(C;T)
Make rs753770252(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome8
Position99832510
GeneVPS13B
is asnp
is mentioned by
dbSNPrs753770252
ebirs753770252
HLIrs753770252
Exacrs753770252
Varsomers753770252
Maprs753770252
PheGenIrs753770252
hapmaprs753770252
1000 genomesrs753770252
hgdprs753770252
ensemblrs753770252
gopubmedrs753770252
geneviewrs753770252
scholarrs753770252
googlers753770252
pharmgkbrs753770252
gwascentralrs753770252
openSNPrs753770252
23andMers753770252
23andMe allrs753770252
SNP Nexus

SNPshotrs753770252
SNPdbers753770252
MSV3drs753770252
GWAS Ctlgrs753770252
Max Magnitude0
ClinVar
Risk rs753770252(G,T;G,T)
Alt rs753770252(G,T;G,T)
Reference rs753770252(C;C)
Significance Pathogenic
Disease Inborn genetic diseases
Variation info
Gene VPS13B
CLNDBN Inborn genetic diseases
Reversed 0
HGVS NC_000008.10:g.100844738C>T
CLNSRC
CLNACC RCV000210619.1,