rs72558201

Orientation

plus

Stabilized

plus

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

Make rs72558201(A;T)

Make rs72558201(T;T)

Reference

GRCh38 38.1/141

Chromosome

10

Position

99836193

Gene

ABCC2

is a	snp
is	mentioned by
dbSNP	rs72558201
dbSNP (classic)	rs72558201
ClinGen	rs72558201
ebi	rs72558201
HLI	rs72558201
Exac	rs72558201
Gnomad	rs72558201
Varsome	rs72558201
LitVar	rs72558201
Map	rs72558201
PheGenI	rs72558201
Biobank	rs72558201
1000 genomes	rs72558201
hgdp	rs72558201
ensembl	rs72558201
geneview	rs72558201
scholar	rs72558201
google	rs72558201
pharmgkb	rs72558201
gwascentral	rs72558201
openSNP	rs72558201
23andMe	rs72558201
SNPshot	rs72558201
SNPdbe	rs72558201
MSV3d	rs72558201
GWAS Ctlg	rs72558201

Max Magnitude

0

OMIM	601107
Desc
Variant	0007
Related	also

ClinVar
Risk	rs72558201(G;G) rs72558201(T;T)
Alt	rs72558201(G;G) rs72558201(T;T)
Reference	Rs72558201(A;A)
Significance	Pathogenic
Disease	Dubin-Johnson syndrome
Variation	info
Gene	ABCC2
CLNDBN	Dubin-Johnson syndrome
Reversed	0
HGVS	NC_000010.10:g.101595950A>T
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000008929.6,