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rs200438844

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs200438844(C;T)
Make rs200438844(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome2
Position26191522
GeneGAREM2, HADHA
is asnp
is mentioned by
dbSNPrs200438844
dbSNP (classic)rs200438844
ClinGenrs200438844
ebirs200438844
HLIrs200438844
Exacrs200438844
Gnomadrs200438844
Varsomers200438844
LitVarrs200438844
Maprs200438844
PheGenIrs200438844
Biobankrs200438844
1000 genomesrs200438844
hgdprs200438844
ensemblrs200438844
geneviewrs200438844
scholarrs200438844
googlers200438844
pharmgkbrs200438844
gwascentralrs200438844
openSNPrs200438844
23andMers200438844
SNPshotrs200438844
SNPdbers200438844
MSV3drs200438844
GWAS Ctlgrs200438844
Max Magnitude0
ClinVar
Risk rs200438844(T;T)
Alt rs200438844(T;T)
Reference Rs200438844(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene HADHA
CLNDBN not provided
Reversed 0
HGVS NC_000002.11:g.26414391C>T
CLNSRC
CLNACC RCV000493353.1,