rs76483862

Orientation

plus

Stabilized

plus

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

Make rs76483862(A;A)

Make rs76483862(A;G)

Reference

GRCh38 38.1/141

Chromosome

4

Position

73416280

Gene

ALB

is a	snp
is	mentioned by
dbSNP	rs76483862
dbSNP (classic)	rs76483862
ClinGen	rs76483862
ebi	rs76483862
HLI	rs76483862
Exac	rs76483862
Gnomad	rs76483862
Varsome	rs76483862
LitVar	rs76483862
Map	rs76483862
PheGenI	rs76483862
Biobank	rs76483862
1000 genomes	rs76483862
hgdp	rs76483862
ensembl	rs76483862
geneview	rs76483862
scholar	rs76483862
google	rs76483862
pharmgkb	rs76483862
gwascentral	rs76483862
openSNP	rs76483862
23andMe	rs76483862
SNPshot	rs76483862
SNPdbe	rs76483862
MSV3d	rs76483862
GWAS Ctlg	rs76483862

Max Magnitude

0

OMIM	103600
Desc
Variant	0018
Related	also

ClinVar
Risk	rs76483862(A;A)
Alt	rs76483862(A;A)
Reference	Rs76483862(G;G)
Significance	Other
Disease	ALBUMIN HIROSHIMA 2
Variation	info
Gene	ALB
CLNDBN	ALBUMIN HIROSHIMA 2
Reversed	0
HGVS	NC_000004.11:g.74281997G>A
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000019848.1,

[PMID 2762316] Point substitutions in Japanese alloalbumins.