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rs796051971

From SNPedia

Orientationminus
Geno Mag Summary
(;) 0 common in clinvar
Make rs796051971(-;-)
Make rs796051971(-;ATCA)
Make rs796051971(ATCA;ATCA)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position26192390
GeneGAREM2, HADHA
is asnp
is mentioned by
dbSNPrs796051971
ebirs796051971
HLIrs796051971
Exacrs796051971
Varsomers796051971
Maprs796051971
PheGenIrs796051971
hapmaprs796051971
1000 genomesrs796051971
hgdprs796051971
ensemblrs796051971
gopubmedrs796051971
geneviewrs796051971
scholarrs796051971
googlers796051971
pharmgkbrs796051971
gwascentralrs796051971
openSNPrs796051971
23andMers796051971
23andMe allrs796051971
SNP Nexus

SNPshotrs796051971
SNPdbers796051971
MSV3drs796051971
GWAS Ctlgrs796051971
Max Magnitude0
ClinVar
Risk rs796051971(ATCA;ATCA)
Alt rs796051971(ATCA;ATCA)
Reference rs796051971(;)
Significance Pathogenic
Disease not provided
Variation info
Gene HADHA
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.26415260_26415263dupTGAT
CLNSRC
CLNACC RCV000185935.1,