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rs75523493

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in complete genomics
Make rs75523493(A;A)
Make rs75523493(A;G)
ReferenceGRCh38 38.1/141
Chromosome4
Position73418232
GeneALB
is asnp
is mentioned by
dbSNPrs75523493
ebirs75523493
HLIrs75523493
Exacrs75523493
Varsomers75523493
Maprs75523493
PheGenIrs75523493
hapmaprs75523493
1000 genomesrs75523493
hgdprs75523493
ensemblrs75523493
gopubmedrs75523493
geneviewrs75523493
scholarrs75523493
googlers75523493
pharmgkbrs75523493
gwascentralrs75523493
openSNPrs75523493
23andMers75523493
23andMe allrs75523493
SNP Nexus

SNPshotrs75523493
SNPdbers75523493
MSV3drs75523493
GWAS Ctlgrs75523493
Max Magnitude0
OMIM103600
Desc
Variant0019
Relatedalso
ClinVar
Risk rs75523493(A;A)
Alt rs75523493(A;A)
Reference rs75523493(G;G)
Significance Other
Disease ALBUMIN VANCOUVER
Variation info
Gene ALB
CLNDBN ALBUMIN VANCOUVER
Reversed 0
HGVS NC_000004.11:g.74283949G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000019851.1,


[PMID 2317208OA-icon.png] Genetic characterization of an alloalbumin, albumin Kashmir, using gene amplification and allele-specific oligonucleotides.


[PMID 2404284OA-icon.png] Point substitutions in albumin genetic variants from Asia.