rs387906869

Orientation

minus

Stabilized

minus

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

Make rs387906869(-;-)

Make rs387906869(-;AC)

Reference

GRCh38 38.1/141

Chromosome

4

Position

88113385

Gene

ABCG2

is a	snp
is	mentioned by
dbSNP	rs387906869
dbSNP (classic)	rs387906869
ClinGen	rs387906869
ebi	rs387906869
HLI	rs387906869
Exac	rs387906869
Gnomad	rs387906869
Varsome	rs387906869
LitVar	rs387906869
Map	rs387906869
PheGenI	rs387906869
Biobank	rs387906869
1000 genomes	rs387906869
hgdp	rs387906869
ensembl	rs387906869
geneview	rs387906869
scholar	rs387906869
google	rs387906869
pharmgkb	rs387906869
gwascentral	rs387906869
openSNP	rs387906869
23andMe	rs387906869
SNPshot	rs387906869
SNPdbe	rs387906869
MSV3d	rs387906869
GWAS Ctlg	rs387906869

Max Magnitude

0

ClinVar
Risk	rs387906869(-;-)
Alt	rs387906869(-;-)
Reference	Rs387906869(AC;AC)
Significance	Other
Disease	Blood group
Variation	info
Gene	ABCG2
CLNDBN	Blood group, Junior system
Reversed	1
HGVS	NC_000004.11:g.89034537_89034538delGT
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000023334.4,