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rs863224237

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs863224237(A;G)
Make rs863224237(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome7
Position144765953
GeneTPK1
is asnp
is mentioned by
dbSNPrs863224237
ebirs863224237
HLIrs863224237
Exacrs863224237
Varsomers863224237
Maprs863224237
PheGenIrs863224237
hapmaprs863224237
1000 genomesrs863224237
hgdprs863224237
ensemblrs863224237
gopubmedrs863224237
geneviewrs863224237
scholarrs863224237
googlers863224237
pharmgkbrs863224237
gwascentralrs863224237
openSNPrs863224237
23andMers863224237
23andMe allrs863224237
SNP Nexus

SNPshotrs863224237
SNPdbers863224237
MSV3drs863224237
GWAS Ctlgrs863224237
Max Magnitude0
ClinVar
Risk rs863224237(G;G)
Alt rs863224237(G;G)
Reference rs863224237(A;A)
Significance Pathogenic
Disease not provided
Variation info
Gene TPK1
CLNDBN not provided
Reversed 1
HGVS NC_000007.13:g.144463046T>C
CLNSRC
CLNACC RCV000195651.2,