rs77158239

Orientation

plus

Stabilized

plus

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

Make rs77158239(-;-)

Make rs77158239(-;C)

Reference

GRCh38 38.1/141

Chromosome

4

Position

73420278

Gene

ALB

is a	snp
is	mentioned by
dbSNP	rs77158239
dbSNP (classic)	rs77158239
ClinGen	rs77158239
ebi	rs77158239
HLI	rs77158239
Exac	rs77158239
Gnomad	rs77158239
Varsome	rs77158239
LitVar	rs77158239
Map	rs77158239
PheGenI	rs77158239
Biobank	rs77158239
1000 genomes	rs77158239
hgdp	rs77158239
ensembl	rs77158239
geneview	rs77158239
scholar	rs77158239
google	rs77158239
pharmgkb	rs77158239
gwascentral	rs77158239
openSNP	rs77158239
23andMe	rs77158239
SNPshot	rs77158239
SNPdbe	rs77158239
MSV3d	rs77158239
GWAS Ctlg	rs77158239

Max Magnitude

0

OMIM	103600
Desc
Variant	0032
Related	also

ClinVar
Risk	rs77158239(-;-)
Alt	rs77158239(-;-)
Reference	Rs77158239(C;C)
Significance	Non-pathogenic
Disease	not specified
Variation	info
Gene	ALB
CLNDBN	not specified
Reversed	0
HGVS	NC_000004.11:g.74285995delC
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000019877.2,

[PMID 2068071] A donor splice mutation and a single-base deletion produce two carboxyl-terminal variants of human serum albumin.

[PMID 3081519] Structural characterization of a chain termination mutant of human serum albumin.