rs79738788

Orientation

plus

Stabilized

plus

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

Make rs79738788(A;G)

Make rs79738788(G;G)

Reference

GRCh38 38.1/141

Chromosome

4

Position

73419575

Gene

ALB

is a	snp
is	mentioned by
dbSNP	rs79738788
dbSNP (classic)	rs79738788
ClinGen	rs79738788
ebi	rs79738788
HLI	rs79738788
Exac	rs79738788
Gnomad	rs79738788
Varsome	rs79738788
LitVar	rs79738788
Map	rs79738788
PheGenI	rs79738788
Biobank	rs79738788
1000 genomes	rs79738788
hgdp	rs79738788
ensembl	rs79738788
geneview	rs79738788
scholar	rs79738788
google	rs79738788
pharmgkb	rs79738788
gwascentral	rs79738788
openSNP	rs79738788
23andMe	rs79738788
SNPshot	rs79738788
SNPdbe	rs79738788
MSV3d	rs79738788
GWAS Ctlg	rs79738788

Max Magnitude

0

OMIM	103600
Desc
Variant	0021
Related	also

ClinVar
Risk	rs79738788(C;C) rs79738788(G;G)
Alt	rs79738788(C;C) rs79738788(G;G)
Reference	Rs79738788(A;A)
Significance	Other
Disease	Alloalbuminemia ALBUMIN MEXICO 2
Variation	info
Gene	ALB
CLNDBN	Alloalbuminemia ALBUMIN MEXICO 2
Reversed	0
HGVS	NC_000004.11:g.74285292A>C; NC_000004.11:g.74285292A>G
CLNSRC	UniProtKB (protein) OMIM Allelic Variant
CLNACC	RCV000144399.1, RCV000019857.1,

[PMID 3474609] Amino acid substitutions in genetic variants of human serum albumin and in sequences inferred from molecular cloning.

[PMID 1518850] Alloalbuminemia in Sweden: structural study and phenotypic distribution of nine albumin variants.