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rs863224176

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs863224176(A;C)
Make rs863224176(C;C)
ReferenceGRCh38.p2 38.2/146
Chromosome12
Position131941625
GenePUS1
is asnp
is mentioned by
dbSNPrs863224176
ebirs863224176
HLIrs863224176
Exacrs863224176
Varsomers863224176
Maprs863224176
PheGenIrs863224176
hapmaprs863224176
1000 genomesrs863224176
hgdprs863224176
ensemblrs863224176
gopubmedrs863224176
geneviewrs863224176
scholarrs863224176
googlers863224176
pharmgkbrs863224176
gwascentralrs863224176
openSNPrs863224176
23andMers863224176
23andMe allrs863224176
SNP Nexus

SNPshotrs863224176
SNPdbers863224176
MSV3drs863224176
GWAS Ctlgrs863224176
Max Magnitude0
ClinVar
Risk rs863224176(C;C)
Alt rs863224176(C;C)
Reference rs863224176(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene PUS1
CLNDBN not provided
Reversed 0
HGVS NC_000012.11:g.132426170A>C
CLNSRC
CLNACC RCV000195831.1,