rs75791663

Orientation

plus

Stabilized

plus

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

Make rs75791663(A;A)

Make rs75791663(A;G)

Reference

GRCh38 38.1/141

Chromosome

4

Position

73415120

Gene

ALB

is a	snp
is	mentioned by
dbSNP	rs75791663
dbSNP (classic)	rs75791663
ClinGen	rs75791663
ebi	rs75791663
HLI	rs75791663
Exac	rs75791663
Gnomad	rs75791663
Varsome	rs75791663
LitVar	rs75791663
Map	rs75791663
PheGenI	rs75791663
Biobank	rs75791663
1000 genomes	rs75791663
hgdp	rs75791663
ensembl	rs75791663
geneview	rs75791663
scholar	rs75791663
google	rs75791663
pharmgkb	rs75791663
gwascentral	rs75791663
openSNP	rs75791663
23andMe	rs75791663
SNPshot	rs75791663
SNPdbe	rs75791663
MSV3d	rs75791663
GWAS Ctlg	rs75791663

Max Magnitude

0

OMIM	103600
Desc
Variant	0013
Related	also

ClinVar
Risk	rs75791663(A;A)
Alt	rs75791663(A;A)
Reference	Rs75791663(G;G)
Significance	Other
Disease	ALBUMIN COARI I
Variation	info
Gene	ALB
CLNDBN	ALBUMIN COARI I
Reversed	0
HGVS	NC_000004.11:g.74280837G>A
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000019840.2,

[PMID 2564675] Amino acid substitutions in albumin variants found in Brazil.