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rs367683258

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs367683258(C;T)
Make rs367683258(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome22
Position46352276
GeneTRMU
is asnp
is mentioned by
dbSNPrs367683258
ebirs367683258
HLIrs367683258
Exacrs367683258
Varsomers367683258
Maprs367683258
PheGenIrs367683258
hapmaprs367683258
1000 genomesrs367683258
hgdprs367683258
ensemblrs367683258
gopubmedrs367683258
geneviewrs367683258
scholarrs367683258
googlers367683258
pharmgkbrs367683258
gwascentralrs367683258
openSNPrs367683258
23andMers367683258
23andMe allrs367683258
SNP Nexus

SNPshotrs367683258
SNPdbers367683258
MSV3drs367683258
GWAS Ctlgrs367683258
Max Magnitude0
ClinVar
Risk rs367683258(G,T;G,T)
Alt rs367683258(G,T;G,T)
Reference rs367683258(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene TRMU
CLNDBN not provided
Reversed 0
HGVS NC_000022.10:g.46748173C>T
CLNSRC
CLNACC RCV000200369.2,