Have questions? Visit https://www.reddit.com/r/SNPedia

rs863224167

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs863224167(A;G)
Make rs863224167(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome6
Position107212111
GenePDSS2
is asnp
is mentioned by
dbSNPrs863224167
ebirs863224167
HLIrs863224167
Exacrs863224167
Varsomers863224167
Maprs863224167
PheGenIrs863224167
hapmaprs863224167
1000 genomesrs863224167
hgdprs863224167
ensemblrs863224167
gopubmedrs863224167
geneviewrs863224167
scholarrs863224167
googlers863224167
pharmgkbrs863224167
gwascentralrs863224167
openSNPrs863224167
23andMers863224167
23andMe allrs863224167
SNP Nexus

SNPshotrs863224167
SNPdbers863224167
MSV3drs863224167
GWAS Ctlgrs863224167
Max Magnitude0
ClinVar
Risk rs863224167(G;G)
Alt rs863224167(G;G)
Reference rs863224167(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene PDSS2
CLNDBN not provided
Reversed 1
HGVS NC_000006.11:g.107533315T>C
CLNSRC
CLNACC RCV000196261.1,