rs75522063

Orientation

plus

Stabilized

plus

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

Make rs75522063(A;A)

Make rs75522063(A;G)

Reference

GRCh38 38.1/141

Chromosome

4

Position

73408750

Gene

ALB

is a	snp
is	mentioned by
dbSNP	rs75522063
dbSNP (classic)	rs75522063
ClinGen	rs75522063
ebi	rs75522063
HLI	rs75522063
Exac	rs75522063
Gnomad	rs75522063
Varsome	rs75522063
LitVar	rs75522063
Map	rs75522063
PheGenI	rs75522063
Biobank	rs75522063
1000 genomes	rs75522063
hgdp	rs75522063
ensembl	rs75522063
geneview	rs75522063
scholar	rs75522063
google	rs75522063
pharmgkb	rs75522063
gwascentral	rs75522063
openSNP	rs75522063
23andMe	rs75522063
SNPshot	rs75522063
SNPdbe	rs75522063
MSV3d	rs75522063
GWAS Ctlg	rs75522063

Max Magnitude

0

OMIM	103600
Desc
Variant	0007
Related	also

ClinVar
Risk	rs75522063(A;A)
Alt	rs75522063(A;A)
Reference	Rs75522063(G;G)
Significance	Other
Disease	ALBUMIN NAGOYA
Variation	info
Gene	ALB
CLNDBN	ALBUMIN NAGOYA
Reversed	0
HGVS	NC_000004.11:g.74274467G>A
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000019831.1,

[PMID 2404284] Point substitutions in albumin genetic variants from Asia.