rs387906596

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(C;C)	0	common in clinvar

Make rs387906596(C;T)

Make rs387906596(T;T)

Reference

GRCh38 38.1/141

Chromosome

7

Position

43788022

Gene	BLVRA, LOC102724946

is a	snp
is	mentioned by
dbSNP	rs387906596
dbSNP (classic)	rs387906596
ClinGen	rs387906596
ebi	rs387906596
HLI	rs387906596
Exac	rs387906596
Gnomad	rs387906596
Varsome	rs387906596
LitVar	rs387906596
Map	rs387906596
PheGenI	rs387906596
Biobank	rs387906596
1000 genomes	rs387906596
hgdp	rs387906596
ensembl	rs387906596
geneview	rs387906596
scholar	rs387906596
google	rs387906596
pharmgkb	rs387906596
gwascentral	rs387906596
openSNP	rs387906596
23andMe	rs387906596
SNPshot	rs387906596
SNPdbe	rs387906596
MSV3d	rs387906596
GWAS Ctlg	rs387906596

Max Magnitude

0

ClinVar
Risk	rs387906596(G;G) rs387906596(T;T)
Alt	rs387906596(G;G) rs387906596(T;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,