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rs180177329

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs180177329(-;-)
Make rs180177329(-;T)
Make rs180177329(T;T)
ReferenceGRCh38 38.1/141
Chromosome8
Position99823832
GeneVPS13B
is asnp
is mentioned by
dbSNPrs180177329
ebirs180177329
HLIrs180177329
Exacrs180177329
Varsomers180177329
Maprs180177329
PheGenIrs180177329
hapmaprs180177329
1000 genomesrs180177329
hgdprs180177329
ensemblrs180177329
gopubmedrs180177329
geneviewrs180177329
scholarrs180177329
googlers180177329
pharmgkbrs180177329
gwascentralrs180177329
openSNPrs180177329
23andMers180177329
23andMe allrs180177329
SNP Nexus

SNPshotrs180177329
SNPdbers180177329
MSV3drs180177329
GWAS Ctlgrs180177329
Max Magnitude0
ClinVar
Risk rs180177329(T;T)
Alt rs180177329(T;T)
Reference rs180177329(;)
Significance Other
Disease Cohen syndrome not provided
Variation info
Gene VPS13B
CLNDBN Cohen syndrome not provided
Reversed 0
HGVS NC_000008.10:g.100836061dupT
CLNSRC OMIM Allelic Variant
CLNACC RCV000002960.7, RCV000058940.1,