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rs397514504

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs397514504(G;T)
Make rs397514504(T;T)
ReferenceGRCh38 38.1/141
Chromosome9
Position133733963
GeneSARDH
is asnp
is mentioned by
dbSNPrs397514504
ebirs397514504
HLIrs397514504
Exacrs397514504
Varsomers397514504
Maprs397514504
PheGenIrs397514504
hapmaprs397514504
1000 genomesrs397514504
hgdprs397514504
ensemblrs397514504
gopubmedrs397514504
geneviewrs397514504
scholarrs397514504
googlers397514504
pharmgkbrs397514504
gwascentralrs397514504
openSNPrs397514504
23andMers397514504
23andMe allrs397514504
SNP Nexus

SNPshotrs397514504
SNPdbers397514504
MSV3drs397514504
GWAS Ctlgrs397514504
Max Magnitude0
ClinVar
Risk rs397514504(T;T)
Alt rs397514504(T;T)
Reference rs397514504(G;G)
Significance Other
Disease Sarcosine dehydrogenase deficiency
Variation info
Gene SARDH
CLNDBN Sarcosine dehydrogenase deficiency
Reversed 1
HGVS NC_000009.11:g.136599085C>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000032643.3,