rs74718349

Orientation

plus

Stabilized

plus

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

Make rs74718349(C;C)

Make rs74718349(C;G)

Reference

GRCh38 38.1/141

Chromosome

4

Position

73413476

Gene

ALB

is a	snp
is	mentioned by
dbSNP	rs74718349
dbSNP (classic)	rs74718349
ClinGen	rs74718349
ebi	rs74718349
HLI	rs74718349
Exac	rs74718349
Gnomad	rs74718349
Varsome	rs74718349
LitVar	rs74718349
Map	rs74718349
PheGenI	rs74718349
Biobank	rs74718349
1000 genomes	rs74718349
hgdp	rs74718349
ensembl	rs74718349
geneview	rs74718349
scholar	rs74718349
google	rs74718349
pharmgkb	rs74718349
gwascentral	rs74718349
openSNP	rs74718349
23andMe	rs74718349
SNPshot	rs74718349
SNPdbe	rs74718349
MSV3d	rs74718349
GWAS Ctlg	rs74718349

Max Magnitude

0

OMIM	103600
Desc
Variant	0044
Related	also

ClinVar
Risk	rs74718349(C;C) rs74718349(T;T)
Alt	rs74718349(C;C) rs74718349(T;T)
Reference	Rs74718349(G;G)
Significance	Other
Disease	ALBUMIN CASERTA
Variation	info
Gene	ALB
CLNDBN	ALBUMIN CASERTA
Reversed	0
HGVS	NC_000004.11:g.74279193G>C
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000019889.1,

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