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rs796051973

From SNPedia

Orientationminus
Geno Mag Summary
(;) 0 common in clinvar
Make rs796051973(-;-)
Make rs796051973(-;TGAAGTC)
Make rs796051973(TGAAGTC;TGAAGTC)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position26194584
GeneGAREM2, HADHA
is asnp
is mentioned by
dbSNPrs796051973
ebirs796051973
HLIrs796051973
Exacrs796051973
Varsomers796051973
Maprs796051973
PheGenIrs796051973
hapmaprs796051973
1000 genomesrs796051973
hgdprs796051973
ensemblrs796051973
gopubmedrs796051973
geneviewrs796051973
scholarrs796051973
googlers796051973
pharmgkbrs796051973
gwascentralrs796051973
openSNPrs796051973
23andMers796051973
23andMe allrs796051973
SNP Nexus

SNPshotrs796051973
SNPdbers796051973
MSV3drs796051973
GWAS Ctlgrs796051973
Max Magnitude0
ClinVar
Risk rs796051973(TGAAGTC;TGAAGTC)
Alt rs796051973(TGAAGTC;TGAAGTC)
Reference rs796051973(;)
Significance Pathogenic
Disease not provided
Variation info
Gene HADHA
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.26417454_26417460dupGACTTCA
CLNSRC
CLNACC RCV000185938.1,