rs752916287

Orientation

plus

Stabilized

plus

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

Make rs752916287(C;G)

Make rs752916287(G;G)

Reference

GRCh38.p2 38.2/144

Chromosome

7

Position

87411911

Gene

ABCB4

is a	snp
is	mentioned by
dbSNP	rs752916287
dbSNP (classic)	rs752916287
ClinGen	rs752916287
ebi	rs752916287
HLI	rs752916287
Exac	rs752916287
Gnomad	rs752916287
Varsome	rs752916287
LitVar	rs752916287
Map	rs752916287
PheGenI	rs752916287
Biobank	rs752916287
1000 genomes	rs752916287
hgdp	rs752916287
ensembl	rs752916287
geneview	rs752916287
scholar	rs752916287
google	rs752916287
pharmgkb	rs752916287
gwascentral	rs752916287
openSNP	rs752916287
23andMe	rs752916287
SNPshot	rs752916287
SNPdbe	rs752916287
MSV3d	rs752916287
GWAS Ctlg	rs752916287

Max Magnitude

0

ClinVar
Risk	rs752916287(G;G) rs752916287(T;T)
Alt	rs752916287(G;G) rs752916287(T;T)
Reference	Rs752916287(C;C)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	ABCB4
CLNDBN	not provided
Reversed	0
HGVS	NC_000007.13:g.87041227C>T
CLNSRC
CLNACC	RCV000171407.1,