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rs863224246

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs863224246(A;G)
Make rs863224246(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome16
Position28843147
GeneLOC105371163, NPIPB8, TUFM
is asnp
is mentioned by
dbSNPrs863224246
ebirs863224246
HLIrs863224246
Exacrs863224246
Varsomers863224246
Maprs863224246
PheGenIrs863224246
hapmaprs863224246
1000 genomesrs863224246
hgdprs863224246
ensemblrs863224246
gopubmedrs863224246
geneviewrs863224246
scholarrs863224246
googlers863224246
pharmgkbrs863224246
gwascentralrs863224246
openSNPrs863224246
23andMers863224246
23andMe allrs863224246
SNP Nexus

SNPshotrs863224246
SNPdbers863224246
MSV3drs863224246
GWAS Ctlgrs863224246
Max Magnitude0
ClinVar
Risk rs863224246(G;G)
Alt rs863224246(G;G)
Reference rs863224246(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene TUFM NPIPB8
CLNDBN not provided
Reversed 1
HGVS NC_000016.9:g.28854468T>C
CLNSRC
CLNACC RCV000199210.1,