rs55722397

Orientation

minus

Stabilized

minus

Geno	Mag	Summary
(C;C)	0	common in complete genomics

Make rs55722397(C;G)

Make rs55722397(G;G)

Reference

GRCh38 38.1/141

Chromosome

9

Position

133256031

Gene

ABO

is a	snp
is	mentioned by
dbSNP	rs55722397
dbSNP (classic)	rs55722397
ClinGen	rs55722397
ebi	rs55722397
HLI	rs55722397
Exac	rs55722397
Gnomad	rs55722397
Varsome	rs55722397
LitVar	rs55722397
Map	rs55722397
PheGenI	rs55722397
Biobank	rs55722397
1000 genomes	rs55722397
hgdp	rs55722397
ensembl	rs55722397
geneview	rs55722397
scholar	rs55722397
google	rs55722397
pharmgkb	rs55722397
gwascentral	rs55722397
openSNP	rs55722397
23andMe	rs55722397
SNPshot	rs55722397
SNPdbe	rs55722397
MSV3d	rs55722397
GWAS Ctlg	rs55722397

Max Magnitude

0

OMIM	110300
Desc
Variant	0005
Related	also

ClinVar
Risk	rs55722397(G;G)
Alt	rs55722397(G;G)
Reference	Rs55722397(C;C)
Significance	Other
Disease	ABO blood group system
Variation	info
Gene	ABO
CLNDBN	ABO blood group system
Reversed	1
HGVS	NC_000009.11:g.136131418G>C
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000019313.29,