rs371866713

Orientation

plus

Stabilized

plus

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

Make rs371866713(C;G)

Make rs371866713(G;G)

Reference

GRCh38.p7 38.3/149

Chromosome

10

Position

99799313

Gene

ABCC2

is a	snp
is	mentioned by
dbSNP	rs371866713
dbSNP (classic)	rs371866713
ClinGen	rs371866713
ebi	rs371866713
HLI	rs371866713
Exac	rs371866713
Gnomad	rs371866713
Varsome	rs371866713
LitVar	rs371866713
Map	rs371866713
PheGenI	rs371866713
Biobank	rs371866713
1000 genomes	rs371866713
hgdp	rs371866713
ensembl	rs371866713
geneview	rs371866713
scholar	rs371866713
google	rs371866713
pharmgkb	rs371866713
gwascentral	rs371866713
openSNP	rs371866713
23andMe	rs371866713
SNPshot	rs371866713
SNPdbe	rs371866713
MSV3d	rs371866713
GWAS Ctlg	rs371866713

Max Magnitude

0

ClinVar
Risk	rs371866713(G;G)
Alt	rs371866713(G;G)
Reference	Rs371866713(C;C)
Significance	Pathogenic
Disease	Dubin-Johnson syndrome
Variation	info
Gene	ABCC2
CLNDBN	Dubin-Johnson syndrome
Reversed	0
HGVS	NC_000010.10:g.101559070C>G
CLNSRC
CLNACC	RCV000343826.1,