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rs148567433

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs148567433(C;T)
Make rs148567433(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome19
Position51353280
GeneETFB
is asnp
is mentioned by
dbSNPrs148567433
ebirs148567433
HLIrs148567433
Exacrs148567433
Varsomers148567433
Maprs148567433
PheGenIrs148567433
hapmaprs148567433
1000 genomesrs148567433
hgdprs148567433
ensemblrs148567433
gopubmedrs148567433
geneviewrs148567433
scholarrs148567433
googlers148567433
pharmgkbrs148567433
gwascentralrs148567433
openSNPrs148567433
23andMers148567433
23andMe allrs148567433
SNP Nexus

SNPshotrs148567433
SNPdbers148567433
MSV3drs148567433
GWAS Ctlgrs148567433
Max Magnitude0
ClinVar
Risk rs148567433(T;T)
Alt rs148567433(T;T)
Reference rs148567433(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene ETFB
CLNDBN not provided
Reversed 0
HGVS NC_000019.9:g.51856534C>T
CLNSRC
CLNACC RCV000185879.2,