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rs770665020

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs770665020(A;G)
Make rs770665020(G;G)
ReferenceGRCh38.p2 38.2/147
Chromosome19
Position51353271
GeneETFB
is asnp
is mentioned by
dbSNPrs770665020
ebirs770665020
HLIrs770665020
Exacrs770665020
Varsomers770665020
Maprs770665020
PheGenIrs770665020
hapmaprs770665020
1000 genomesrs770665020
hgdprs770665020
ensemblrs770665020
gopubmedrs770665020
geneviewrs770665020
scholarrs770665020
googlers770665020
pharmgkbrs770665020
gwascentralrs770665020
openSNPrs770665020
23andMers770665020
23andMe allrs770665020
SNP Nexus

SNPshotrs770665020
SNPdbers770665020
MSV3drs770665020
GWAS Ctlgrs770665020
Max Magnitude0
ClinVar
Risk rs770665020(G;G)
Alt rs770665020(G;G)
Reference rs770665020(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene ETFB
CLNDBN not provided
Reversed 0
HGVS NC_000019.9:g.51856525A>T
CLNSRC
CLNACC RCV000185881.2,