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rs75522063

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in complete genomics
Make rs75522063(A;A)
Make rs75522063(A;G)
ReferenceGRCh38 38.1/141
Chromosome4
Position73408750
GeneALB
is asnp
is mentioned by
dbSNPrs75522063
ebirs75522063
HLIrs75522063
Exacrs75522063
Varsomers75522063
Maprs75522063
PheGenIrs75522063
hapmaprs75522063
1000 genomesrs75522063
hgdprs75522063
ensemblrs75522063
gopubmedrs75522063
geneviewrs75522063
scholarrs75522063
googlers75522063
pharmgkbrs75522063
gwascentralrs75522063
openSNPrs75522063
23andMers75522063
23andMe allrs75522063
SNP Nexus

SNPshotrs75522063
SNPdbers75522063
MSV3drs75522063
GWAS Ctlgrs75522063
Max Magnitude0
OMIM103600
Desc
Variant0007
Relatedalso
ClinVar
Risk rs75522063(A;A)
Alt rs75522063(A;A)
Reference rs75522063(G;G)
Significance Other
Disease ALBUMIN NAGOYA
Variation info
Gene ALB
CLNDBN ALBUMIN NAGOYA
Reversed 0
HGVS NC_000004.11:g.74274467G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000019831.1,


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