rs1800580

Orientation

plus

Stabilized

plus

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

Make rs1800580(C;C)

Make rs1800580(C;G)

Reference

GRCh38 38.1/141

Chromosome

4

Position

73419640

Gene

ALB

is a	snp
is	mentioned by
dbSNP	rs1800580
dbSNP (classic)	rs1800580
ClinGen	rs1800580
ebi	rs1800580
HLI	rs1800580
Exac	rs1800580
Gnomad	rs1800580
Varsome	rs1800580
LitVar	rs1800580
Map	rs1800580
PheGenI	rs1800580
Biobank	rs1800580
1000 genomes	rs1800580
hgdp	rs1800580
ensembl	rs1800580
geneview	rs1800580
scholar	rs1800580
google	rs1800580
pharmgkb	rs1800580
gwascentral	rs1800580
openSNP	rs1800580
23andMe	rs1800580
SNPshot	rs1800580
SNPdbe	rs1800580
MSV3d	rs1800580
GWAS Ctlg	rs1800580

Max Magnitude

0

OMIM	103600
Desc
Variant	0038
Related	also

ClinVar
Risk	rs1800580(C;C)
Alt	rs1800580(C;C)
Reference	Rs1800580(G;G)
Significance	Other
Disease	ALBUMIN RUGBY PARK
Variation	info
Gene	ALB
CLNDBN	ALBUMIN RUGBY PARK
Reversed	0
HGVS	NC_000004.11:g.74285357G>C
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000019883.1,

[PMID 1390939] Albumin Rugby Park: a truncated albumin variant caused by a G-->C splice-site mutation in intron 13.

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