rs72558199

Orientation

plus

Stabilized

plus

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

Make rs72558199(C;T)

Make rs72558199(T;T)

Reference

GRCh38 38.1/141

Chromosome

10

Position

99832069

Gene

ABCC2

is a	snp
is	mentioned by
dbSNP	rs72558199
dbSNP (classic)	rs72558199
ClinGen	rs72558199
ebi	rs72558199
HLI	rs72558199
Exac	rs72558199
Gnomad	rs72558199
Varsome	rs72558199
LitVar	rs72558199
Map	rs72558199
PheGenI	rs72558199
Biobank	rs72558199
1000 genomes	rs72558199
hgdp	rs72558199
ensembl	rs72558199
geneview	rs72558199
scholar	rs72558199
google	rs72558199
pharmgkb	rs72558199
gwascentral	rs72558199
openSNP	rs72558199
23andMe	rs72558199
SNPshot	rs72558199
SNPdbe	rs72558199
MSV3d	rs72558199
GWAS Ctlg	rs72558199

Max Magnitude

0

ClinVar
Risk	rs72558199(T;T)
Alt	rs72558199(T;T)
Reference	Rs72558199(C;C)
Significance	Other
Disease	Dubin-Johnson syndrome
Variation	info
Gene	ABCC2
CLNDBN	Dubin-Johnson syndrome
Reversed	0
HGVS	NC_000010.10:g.101591826C>T
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000024307.5,