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rs796051963

From SNPedia

Orientationplus
Geno Mag Summary
(CAGGTAAGGTATAGTGA;CAGGTAAGGTATAGTGA) 0 common in clinvar
Make rs796051963(CAGGTAAGGTATAGTGA;T)
Make rs796051963(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome4
Position158684671
GeneETFDH
is asnp
is mentioned by
dbSNPrs796051963
ClinGenrs796051963
ebirs796051963
HLIrs796051963
Exacrs796051963
Varsomers796051963
Maprs796051963
PheGenIrs796051963
hapmaprs796051963
1000 genomesrs796051963
hgdprs796051963
ensemblrs796051963
gopubmedrs796051963
geneviewrs796051963
scholarrs796051963
googlers796051963
pharmgkbrs796051963
gwascentralrs796051963
openSNPrs796051963
23andMers796051963
23andMe allrs796051963
SNP Nexus

SNPshotrs796051963
SNPdbers796051963
MSV3drs796051963
GWAS Ctlgrs796051963
Max Magnitude0
ClinVar
Risk rs796051963(T;T)
Alt rs796051963(T;T)
Reference Rs796051963(CAGGTAAGGTATAGTGA;CAGGTAAGGTATAGTGA)
Significance Pathogenic
Disease not provided
Variation info
Gene ETFDH
CLNDBN not provided
Reversed 0
HGVS NC_000004.11:g.159605823_159605839del17insT
CLNSRC
CLNACC RCV000185905.1,