rs200190472

Orientation

minus

Stabilized

minus

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

Make rs200190472(C;T)

Make rs200190472(T;T)

Reference

GRCh38 38.1/141

Chromosome

4

Position

88118214

Gene

ABCG2

is a	snp
is	mentioned by
dbSNP	rs200190472
dbSNP (classic)	rs200190472
ClinGen	rs200190472
ebi	rs200190472
HLI	rs200190472
Exac	rs200190472
Gnomad	rs200190472
Varsome	rs200190472
LitVar	rs200190472
Map	rs200190472
PheGenI	rs200190472
Biobank	rs200190472
1000 genomes	rs200190472
hgdp	rs200190472
ensembl	rs200190472
geneview	rs200190472
scholar	rs200190472
google	rs200190472
pharmgkb	rs200190472
gwascentral	rs200190472
openSNP	rs200190472
23andMe	rs200190472
SNPshot	rs200190472
SNPdbe	rs200190472
MSV3d	rs200190472
GWAS Ctlg	rs200190472

Max Magnitude

0

ClinVar
Risk	rs200190472(T;T)
Alt	rs200190472(T;T)
Reference	Rs200190472(C;C)
Significance	Other
Disease	Blood group
Variation	info
Gene	ABCG2
CLNDBN	Blood group, Junior system
Reversed	1
HGVS	NC_000004.11:g.89039366G>A
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000023333.4,