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rs75709682

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in complete genomics
Make rs75709682(A;A)
Make rs75709682(A;G)
ReferenceGRCh38 38.1/141
Chromosome4
Position73419619
GeneALB
is asnp
is mentioned by
dbSNPrs75709682
ebirs75709682
HLIrs75709682
Exacrs75709682
Varsomers75709682
Maprs75709682
PheGenIrs75709682
hapmaprs75709682
1000 genomesrs75709682
hgdprs75709682
ensemblrs75709682
gopubmedrs75709682
geneviewrs75709682
scholarrs75709682
googlers75709682
pharmgkbrs75709682
gwascentralrs75709682
openSNPrs75709682
23andMers75709682
23andMe allrs75709682
SNP Nexus

SNPshotrs75709682
SNPdbers75709682
MSV3drs75709682
GWAS Ctlgrs75709682
Max Magnitude0
OMIM103600
Desc
Variant0023
Relatedalso
ClinVar
Risk rs75709682(A;A)
Alt rs75709682(A;A)
Reference rs75709682(G;G)
Significance Other
Disease ALBUMIN OSAKA 1
Variation info
Gene ALB
CLNDBN ALBUMIN OSAKA 1
Reversed 0
HGVS NC_000004.11:g.74285336G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000019859.1,


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