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rs118203896

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs118203896(A;C)
Make rs118203896(C;C)
ReferenceGRCh38 38.1/141
Chromosome12
Position21643971
GeneLDHB
is asnp
is mentioned by
dbSNPrs118203896
ebirs118203896
HLIrs118203896
Exacrs118203896
Varsomers118203896
Maprs118203896
PheGenIrs118203896
hapmaprs118203896
1000 genomesrs118203896
hgdprs118203896
ensemblrs118203896
gopubmedrs118203896
geneviewrs118203896
scholarrs118203896
googlers118203896
pharmgkbrs118203896
gwascentralrs118203896
openSNPrs118203896
23andMers118203896
23andMe allrs118203896
SNP Nexus

SNPshotrs118203896
SNPdbers118203896
MSV3drs118203896
GWAS Ctlgrs118203896
Max Magnitude0
OMIM150100
Desc
Variant0002
Relatedalso
ClinVar
Risk rs118203896(C;C)
Alt rs118203896(C;C)
Reference rs118203896(A;A)
Significance Other
Disease Lactate dehydrogenase B deficiency
Variation info
Gene LDHB
CLNDBN Lactate dehydrogenase B deficiency
Reversed 1
HGVS NC_000012.11:g.21796905T>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000015664.27,