rs76593094

Orientation

plus

Stabilized

plus

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

Make rs76593094(A;A)

Make rs76593094(A;G)

Reference

GRCh38 38.1/141

Chromosome

4

Position

73415108

Gene

ALB

is a	snp
is	mentioned by
dbSNP	rs76593094
dbSNP (classic)	rs76593094
ClinGen	rs76593094
ebi	rs76593094
HLI	rs76593094
Exac	rs76593094
Gnomad	rs76593094
Varsome	rs76593094
LitVar	rs76593094
Map	rs76593094
PheGenI	rs76593094
Biobank	rs76593094
1000 genomes	rs76593094
hgdp	rs76593094
ensembl	rs76593094
geneview	rs76593094
scholar	rs76593094
google	rs76593094
pharmgkb	rs76593094
gwascentral	rs76593094
openSNP	rs76593094
23andMe	rs76593094
SNPshot	rs76593094
SNPdbe	rs76593094
MSV3d	rs76593094
GWAS Ctlg	rs76593094

Max Magnitude

0

OMIM	103600
Desc
Variant	0012
Related	also

ClinVar
Risk	rs76593094(A;A)
Alt	rs76593094(A;A)
Reference	Rs76593094(G;G)
Significance	Other
Disease	ALBUMIN HIROSHIMA 1
Variation	info
Gene	ALB
CLNDBN	ALBUMIN HIROSHIMA 1
Reversed	0
HGVS	NC_000004.11:g.74280825G>A
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000019839.1,

[PMID 2762316] Point substitutions in Japanese alloalbumins.