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rs75791663

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in complete genomics
Make rs75791663(A;A)
Make rs75791663(A;G)
ReferenceGRCh38 38.1/141
Chromosome4
Position73415120
GeneALB
is asnp
is mentioned by
dbSNPrs75791663
ebirs75791663
HLIrs75791663
Exacrs75791663
Varsomers75791663
Maprs75791663
PheGenIrs75791663
hapmaprs75791663
1000 genomesrs75791663
hgdprs75791663
ensemblrs75791663
gopubmedrs75791663
geneviewrs75791663
scholarrs75791663
googlers75791663
pharmgkbrs75791663
gwascentralrs75791663
openSNPrs75791663
23andMers75791663
23andMe allrs75791663
SNP Nexus

SNPshotrs75791663
SNPdbers75791663
MSV3drs75791663
GWAS Ctlgrs75791663
Max Magnitude0
OMIM103600
Desc
Variant0013
Relatedalso
ClinVar
Risk rs75791663(A;A)
Alt rs75791663(A;A)
Reference rs75791663(G;G)
Significance Other
Disease ALBUMIN COARI I
Variation info
Gene ALB
CLNDBN ALBUMIN COARI I
Reversed 0
HGVS NC_000004.11:g.74280837G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000019840.2,


[PMID 2564675OA-icon.png] Amino acid substitutions in albumin variants found in Brazil.