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rs387906596

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs387906596(C;T)
Make rs387906596(T;T)
ReferenceGRCh38 38.1/141
Chromosome7
Position43788022
GeneBLVRA
is asnp
is mentioned by
dbSNPrs387906596
ebirs387906596
HLIrs387906596
Exacrs387906596
Varsomers387906596
Maprs387906596
PheGenIrs387906596
hapmaprs387906596
1000 genomesrs387906596
hgdprs387906596
ensemblrs387906596
gopubmedrs387906596
geneviewrs387906596
scholarrs387906596
googlers387906596
pharmgkbrs387906596
gwascentralrs387906596
openSNPrs387906596
23andMers387906596
23andMe allrs387906596
SNP Nexus

SNPshotrs387906596
SNPdbers387906596
MSV3drs387906596
GWAS Ctlgrs387906596
Max Magnitude0
ClinVar
Risk rs387906596(G,T;G,T)
Alt rs387906596(G,T;G,T)
Reference rs387906596(C;C)
Significance Pathogenic
Disease Hyperbiliverdinemia
Variation info
Gene BLVRA
CLNDBN Hyperbiliverdinemia
Reversed 0
HGVS NC_000007.13:g.43827621C>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000022452.27,