rs387906870

Orientation

minus

Stabilized

minus

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

Make rs387906870(-;-)

Make rs387906870(-;TT)

Reference

GRCh38 38.1/141

Chromosome

4

Position

88118158

Gene

ABCG2

is a	snp
is	mentioned by
dbSNP	rs387906870
dbSNP (classic)	rs387906870
ClinGen	rs387906870
ebi	rs387906870
HLI	rs387906870
Exac	rs387906870
Gnomad	rs387906870
Varsome	rs387906870
LitVar	rs387906870
Map	rs387906870
PheGenI	rs387906870
Biobank	rs387906870
1000 genomes	rs387906870
hgdp	rs387906870
ensembl	rs387906870
geneview	rs387906870
scholar	rs387906870
google	rs387906870
pharmgkb	rs387906870
gwascentral	rs387906870
openSNP	rs387906870
23andMe	rs387906870
SNPshot	rs387906870
SNPdbe	rs387906870
MSV3d	rs387906870
GWAS Ctlg	rs387906870

Max Magnitude

0

ClinVar
Risk	rs387906870(-;-)
Alt	rs387906870(-;-)
Reference	Rs387906870(TT;TT)
Significance	Other
Disease	Blood group
Variation	info
Gene	ABCG2
CLNDBN	Blood group, Junior system
Reversed	1
HGVS	NC_000004.11:g.89039310_89039311delAA
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000023340.4,