rs75738598

Orientation

plus

Stabilized

plus

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

Make rs75738598(A;C)

Make rs75738598(C;C)

Reference

GRCh38 38.1/141

Chromosome

4

Position

73420262

Gene

ALB

is a	snp
is	mentioned by
dbSNP	rs75738598
dbSNP (classic)	rs75738598
ClinGen	rs75738598
ebi	rs75738598
HLI	rs75738598
Exac	rs75738598
Gnomad	rs75738598
Varsome	rs75738598
LitVar	rs75738598
Map	rs75738598
PheGenI	rs75738598
Biobank	rs75738598
1000 genomes	rs75738598
hgdp	rs75738598
ensembl	rs75738598
geneview	rs75738598
scholar	rs75738598
google	rs75738598
pharmgkb	rs75738598
gwascentral	rs75738598
openSNP	rs75738598
23andMe	rs75738598
SNPshot	rs75738598
SNPdbe	rs75738598
MSV3d	rs75738598
GWAS Ctlg	rs75738598

Max Magnitude

0

OMIM	103600
Desc
Variant	0026
Related	also

ClinVar
Risk	rs75738598(C;C) rs75738598(T;T)
Alt	rs75738598(C;C) rs75738598(T;T)
Reference	Rs75738598(A;A)
Significance	Other
Disease	ALBUMIN VANVES
Variation	info
Gene	ALB
CLNDBN	ALBUMIN VANVES
Reversed	0
HGVS	NC_000004.12:g.73420262A>Y
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000019868.1,

[PMID 3689800] Structural characterization of two genetic variants of human serum albumin.