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rs796051954

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs796051954(A;A)
Make rs796051954(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome19
Position51354206
GeneETFB
is asnp
is mentioned by
dbSNPrs796051954
ebirs796051954
HLIrs796051954
Exacrs796051954
Varsomers796051954
Maprs796051954
PheGenIrs796051954
hapmaprs796051954
1000 genomesrs796051954
hgdprs796051954
ensemblrs796051954
gopubmedrs796051954
geneviewrs796051954
scholarrs796051954
googlers796051954
pharmgkbrs796051954
gwascentralrs796051954
openSNPrs796051954
23andMers796051954
23andMe allrs796051954
SNP Nexus

SNPshotrs796051954
SNPdbers796051954
MSV3drs796051954
GWAS Ctlgrs796051954
Max Magnitude0
ClinVar
Risk rs796051954(A;A)
Alt rs796051954(A;A)
Reference rs796051954(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene ETFB
CLNDBN not provided
Reversed 1
HGVS NC_000019.9:g.51857460C>T
CLNSRC
CLNACC RCV000185878.1,