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rs387906595

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs387906595(C;T)
Make rs387906595(T;T)
ReferenceGRCh38 38.1/141
Chromosome7
Position43787943
GeneBLVRA
is asnp
is mentioned by
dbSNPrs387906595
ebirs387906595
HLIrs387906595
Exacrs387906595
Varsomers387906595
Maprs387906595
PheGenIrs387906595
hapmaprs387906595
1000 genomesrs387906595
hgdprs387906595
ensemblrs387906595
gopubmedrs387906595
geneviewrs387906595
scholarrs387906595
googlers387906595
pharmgkbrs387906595
gwascentralrs387906595
openSNPrs387906595
23andMers387906595
23andMe allrs387906595
SNP Nexus

SNPshotrs387906595
SNPdbers387906595
MSV3drs387906595
GWAS Ctlgrs387906595
Max Magnitude0
ClinVar
Risk rs387906595(T;T)
Alt rs387906595(T;T)
Reference rs387906595(C;C)
Significance Pathogenic
Disease Hyperbiliverdinemia
Variation info
Gene BLVRA
CLNDBN Hyperbiliverdinemia
Reversed 0
HGVS NC_000007.13:g.43827542C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000022451.27,