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rs863224166

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs863224166(A;G)
Make rs863224166(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome6
Position107210572
GenePDSS2
is asnp
is mentioned by
dbSNPrs863224166
ebirs863224166
HLIrs863224166
Exacrs863224166
Varsomers863224166
Maprs863224166
PheGenIrs863224166
hapmaprs863224166
1000 genomesrs863224166
hgdprs863224166
ensemblrs863224166
gopubmedrs863224166
geneviewrs863224166
scholarrs863224166
googlers863224166
pharmgkbrs863224166
gwascentralrs863224166
openSNPrs863224166
23andMers863224166
23andMe allrs863224166
SNP Nexus

SNPshotrs863224166
SNPdbers863224166
MSV3drs863224166
GWAS Ctlgrs863224166
Max Magnitude0
ClinVar
Risk rs863224166(G;G)
Alt rs863224166(G;G)
Reference rs863224166(A;A)
Significance Pathogenic
Disease not provided
Variation info
Gene PDSS2
CLNDBN not provided
Reversed 1
HGVS NC_000006.11:g.107531776T>C
CLNSRC
CLNACC RCV000199826.2,