rs387906395

Orientation

plus

Stabilized

plus

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

Make rs387906395(A;A)

Make rs387906395(A;T)

Reference

GRCh38 38.1/141

Chromosome

10

Position

99808231

Gene

ABCC2

is a	snp
is	mentioned by
dbSNP	rs387906395
dbSNP (classic)	rs387906395
ClinGen	rs387906395
ebi	rs387906395
HLI	rs387906395
Exac	rs387906395
Gnomad	rs387906395
Varsome	rs387906395
LitVar	rs387906395
Map	rs387906395
PheGenI	rs387906395
Biobank	rs387906395
1000 genomes	rs387906395
hgdp	rs387906395
ensembl	rs387906395
geneview	rs387906395
scholar	rs387906395
google	rs387906395
pharmgkb	rs387906395
gwascentral	rs387906395
openSNP	rs387906395
23andMe	rs387906395
SNPshot	rs387906395
SNPdbe	rs387906395
MSV3d	rs387906395
GWAS Ctlg	rs387906395

Max Magnitude

0

ClinVar
Risk	rs387906395(A;A) rs387906395(G;G)
Alt	rs387906395(A;A) rs387906395(G;G)
Reference	Rs387906395(T;T)
Significance	Pathogenic
Disease	Dubin-Johnson syndrome
Variation	info
Gene	ABCC2
CLNDBN	Dubin-Johnson syndrome
Reversed	0
HGVS	NC_000010.10:g.101567988T>A
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000008925.3,