rs764958537

Orientation

plus

Stabilized

plus

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

Make rs764958537(C;C)

Make rs764958537(C;T)

Reference

GRCh38.p7 38.3/149

Chromosome

10

Position

99817338

Gene

ABCC2

is a	snp
is	mentioned by
dbSNP	rs764958537
dbSNP (classic)	rs764958537
ClinGen	rs764958537
ebi	rs764958537
HLI	rs764958537
Exac	rs764958537
Gnomad	rs764958537
Varsome	rs764958537
LitVar	rs764958537
Map	rs764958537
PheGenI	rs764958537
Biobank	rs764958537
1000 genomes	rs764958537
hgdp	rs764958537
ensembl	rs764958537
geneview	rs764958537
scholar	rs764958537
google	rs764958537
pharmgkb	rs764958537
gwascentral	rs764958537
openSNP	rs764958537
23andMe	rs764958537
SNPshot	rs764958537
SNPdbe	rs764958537
MSV3d	rs764958537
GWAS Ctlg	rs764958537

Max Magnitude

0

ClinVar
Risk	rs764958537(C;C)
Alt	rs764958537(C;C)
Reference	Rs764958537(T;T)
Significance	Pathogenic
Disease	Dubin-Johnson syndrome
Variation	info
Gene	ABCC2
CLNDBN	Dubin-Johnson syndrome
Reversed	0
HGVS	NC_000010.10:g.101577095T>C
CLNSRC
CLNACC	RCV000391369.1,