rs387906396

Orientation

plus

Stabilized

plus

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

Make rs387906396(C;C)

Make rs387906396(C;T)

Reference

GRCh38 38.1/141

Chromosome

10

Position

99811604

Gene

ABCC2

is a	snp
is	mentioned by
dbSNP	rs387906396
dbSNP (classic)	rs387906396
ClinGen	rs387906396
ebi	rs387906396
HLI	rs387906396
Exac	rs387906396
Gnomad	rs387906396
Varsome	rs387906396
LitVar	rs387906396
Map	rs387906396
PheGenI	rs387906396
Biobank	rs387906396
1000 genomes	rs387906396
hgdp	rs387906396
ensembl	rs387906396
geneview	rs387906396
scholar	rs387906396
google	rs387906396
pharmgkb	rs387906396
gwascentral	rs387906396
openSNP	rs387906396
23andMe	rs387906396
SNPshot	rs387906396
SNPdbe	rs387906396
MSV3d	rs387906396
GWAS Ctlg	rs387906396

Max Magnitude

0

ClinVar
Risk	rs387906396(C;C)
Alt	rs387906396(C;C)
Reference	Rs387906396(T;T)
Significance	Pathogenic
Disease	Dubin-Johnson syndrome
Variation	info
Gene	ABCC2
CLNDBN	Dubin-Johnson syndrome
Reversed	0
HGVS	NC_000010.10:g.101571361T>C
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000008928.4,