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rs118203895

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs118203895(A;A)
Make rs118203895(A;G)
ReferenceGRCh38 38.1/141
Chromosome12
Position21642032
GeneLDHB
is asnp
is mentioned by
dbSNPrs118203895
ebirs118203895
HLIrs118203895
Exacrs118203895
Varsomers118203895
Maprs118203895
PheGenIrs118203895
hapmaprs118203895
1000 genomesrs118203895
hgdprs118203895
ensemblrs118203895
gopubmedrs118203895
geneviewrs118203895
scholarrs118203895
googlers118203895
pharmgkbrs118203895
gwascentralrs118203895
openSNPrs118203895
23andMers118203895
23andMe allrs118203895
SNP Nexus

SNPshotrs118203895
SNPdbers118203895
MSV3drs118203895
GWAS Ctlgrs118203895
Max Magnitude0
OMIM150100
Desc
Variant0001
Relatedalso
ClinVar
Risk rs118203895(A;A)
Alt rs118203895(A;A)
Reference rs118203895(G;G)
Significance Other
Disease Lactate dehydrogenase B deficiency
Variation info
Gene LDHB
CLNDBN Lactate dehydrogenase B deficiency
Reversed 1
HGVS NC_000012.11:g.21794966C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000015663.27,