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rs863224162

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs863224162(G;T)
Make rs863224162(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome10
Position26705399
GenePDSS1
is asnp
is mentioned by
dbSNPrs863224162
ebirs863224162
HLIrs863224162
Exacrs863224162
Varsomers863224162
Maprs863224162
PheGenIrs863224162
hapmaprs863224162
1000 genomesrs863224162
hgdprs863224162
ensemblrs863224162
gopubmedrs863224162
geneviewrs863224162
scholarrs863224162
googlers863224162
pharmgkbrs863224162
gwascentralrs863224162
openSNPrs863224162
23andMers863224162
23andMe allrs863224162
SNP Nexus

SNPshotrs863224162
SNPdbers863224162
MSV3drs863224162
GWAS Ctlgrs863224162
Max Magnitude0
ClinVar
Risk rs863224162(T;T)
Alt rs863224162(T;T)
Reference rs863224162(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene PDSS1
CLNDBN not provided
Reversed 0
HGVS NC_000010.10:g.26994328G>T
CLNSRC
CLNACC RCV000197300.2,