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rs121434328

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121434328(G;T)
Make rs121434328(T;T)
ReferenceGRCh38 38.1/141
Chromosome12
Position95992772
GeneHAL
is asnp
is mentioned by
dbSNPrs121434328
ebirs121434328
HLIrs121434328
Exacrs121434328
Varsomers121434328
Maprs121434328
PheGenIrs121434328
hapmaprs121434328
1000 genomesrs121434328
hgdprs121434328
ensemblrs121434328
gopubmedrs121434328
geneviewrs121434328
scholarrs121434328
googlers121434328
pharmgkbrs121434328
gwascentralrs121434328
openSNPrs121434328
23andMers121434328
23andMe allrs121434328
SNP Nexus

SNPshotrs121434328
SNPdbers121434328
MSV3drs121434328
GWAS Ctlgrs121434328
Max Magnitude0
OMIM609457
Desc
Variant0002
Relatedalso
ClinVar
Risk rs121434328(A,T;A,T)
Alt rs121434328(A,T;A,T)
Reference rs121434328(G;G)
Significance Other
Disease Histidinemia
Variation info
Gene HAL
CLNDBN Histidinemia
Reversed 1
HGVS NC_000012.11:g.96386550C>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000001758.3,