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rs267607212

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs267607212(C;C)
Make rs267607212(C;T)
ReferenceGRCh38 38.1/141
Chromosome12
Position21635574
GeneLDHB
is asnp
is mentioned by
dbSNPrs267607212
ebirs267607212
HLIrs267607212
Exacrs267607212
Varsomers267607212
Maprs267607212
PheGenIrs267607212
hapmaprs267607212
1000 genomesrs267607212
hgdprs267607212
ensemblrs267607212
gopubmedrs267607212
geneviewrs267607212
scholarrs267607212
googlers267607212
pharmgkbrs267607212
gwascentralrs267607212
openSNPrs267607212
23andMers267607212
23andMe allrs267607212
SNP Nexus

SNPshotrs267607212
SNPdbers267607212
MSV3drs267607212
GWAS Ctlgrs267607212
Max Magnitude0
ClinVar
Risk rs267607212(C;C)
Alt rs267607212(C;C)
Reference rs267607212(T;T)
Significance Other
Disease Lactate dehydrogenase B deficiency
Variation info
Gene LDHB
CLNDBN Lactate dehydrogenase B deficiency
Reversed 1
HGVS NC_000012.11:g.21788508A>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000015666.26,