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rs863224239

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs863224239(G;T)
Make rs863224239(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome22
Position46350350
GeneTRMU
is asnp
is mentioned by
dbSNPrs863224239
ebirs863224239
HLIrs863224239
Exacrs863224239
Varsomers863224239
Maprs863224239
PheGenIrs863224239
hapmaprs863224239
1000 genomesrs863224239
hgdprs863224239
ensemblrs863224239
gopubmedrs863224239
geneviewrs863224239
scholarrs863224239
googlers863224239
pharmgkbrs863224239
gwascentralrs863224239
openSNPrs863224239
23andMers863224239
23andMe allrs863224239
SNP Nexus

SNPshotrs863224239
SNPdbers863224239
MSV3drs863224239
GWAS Ctlgrs863224239
Max Magnitude0
ClinVar
Risk rs863224239(T;T)
Alt rs863224239(T;T)
Reference rs863224239(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene TRMU
CLNDBN not provided
Reversed 0
HGVS NC_000022.10:g.46746247G>T
CLNSRC
CLNACC RCV000198478.1,