rs786205465

Orientation

plus

Stabilized

plus

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

Make rs786205465(G;T)

Make rs786205465(T;T)

Reference

GRCh38.p2 38.2/146

Chromosome

10

Position

99818791

Gene

ABCC2

is a	snp
is	mentioned by
dbSNP	rs786205465
dbSNP (classic)	rs786205465
ClinGen	rs786205465
ebi	rs786205465
HLI	rs786205465
Exac	rs786205465
Gnomad	rs786205465
Varsome	rs786205465
LitVar	rs786205465
Map	rs786205465
PheGenI	rs786205465
Biobank	rs786205465
1000 genomes	rs786205465
hgdp	rs786205465
ensembl	rs786205465
geneview	rs786205465
scholar	rs786205465
google	rs786205465
pharmgkb	rs786205465
gwascentral	rs786205465
openSNP	rs786205465
23andMe	rs786205465
SNPshot	rs786205465
SNPdbe	rs786205465
MSV3d	rs786205465
GWAS Ctlg	rs786205465

Max Magnitude

0

ClinVar
Risk	rs786205465(T;T)
Alt	rs786205465(T;T)
Reference	Rs786205465(G;G)
Significance	Probable-Pathogenic
Disease	not provided Dubin-Johnson syndrome
Variation	info
Gene	ABCC2
CLNDBN	not provided Dubin-Johnson syndrome
Reversed	0
HGVS	NC_000010.10:g.101578548G>T
CLNSRC
CLNACC	RCV000171189.1, RCV000305954.1,