rs74674594

Orientation

plus

Stabilized

plus

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

Make rs74674594(-;-)

Make rs74674594(-;T)

Reference

GRCh38 38.1/141

Chromosome

4

Position

73419625

Gene

ALB

is a	snp
is	mentioned by
dbSNP	rs74674594
dbSNP (classic)	rs74674594
ClinGen	rs74674594
ebi	rs74674594
HLI	rs74674594
Exac	rs74674594
Gnomad	rs74674594
Varsome	rs74674594
LitVar	rs74674594
Map	rs74674594
PheGenI	rs74674594
Biobank	rs74674594
1000 genomes	rs74674594
hgdp	rs74674594
ensembl	rs74674594
geneview	rs74674594
scholar	rs74674594
google	rs74674594
pharmgkb	rs74674594
gwascentral	rs74674594
openSNP	rs74674594
23andMe	rs74674594
SNPshot	rs74674594
SNPdbe	rs74674594
MSV3d	rs74674594
GWAS Ctlg	rs74674594

Max Magnitude

0

OMIM	103600
Desc
Variant	0045
Related	also

ClinVar
Risk	rs74674594(-;-)
Alt	rs74674594(-;-)
Reference	Rs74674594(T;T)
Significance	Other
Disease	ALBUMIN BAZZANO
Variation	info
Gene	ALB
CLNDBN	ALBUMIN BAZZANO
Reversed	0
HGVS	NC_000004.11:g.74285342delT
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000019890.2,

[PMID 8022807] Genetic variants of human serum albumin in Italy: point mutants and a carboxyl-terminal variant.

[PMID 9392528] Effect of genetic variation on the fatty acid-binding properties of human serum albumin and proalbumin.