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rs78574148

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in complete genomics
Make rs78574148(A;A)
Make rs78574148(A;G)
ReferenceGRCh38 38.1/141
Chromosome4
Position73406750
GeneALB
is asnp
is mentioned by
dbSNPrs78574148
ebirs78574148
HLIrs78574148
Exacrs78574148
Varsomers78574148
Maprs78574148
PheGenIrs78574148
hapmaprs78574148
1000 genomesrs78574148
hgdprs78574148
ensemblrs78574148
gopubmedrs78574148
geneviewrs78574148
scholarrs78574148
googlers78574148
pharmgkbrs78574148
gwascentralrs78574148
openSNPrs78574148
23andMers78574148
23andMe allrs78574148
SNP Nexus

SNPshotrs78574148
SNPdbers78574148
MSV3drs78574148
GWAS Ctlgrs78574148
Max Magnitude0
OMIM103600
Desc
Variant0047
Relatedalso
ClinVar
Risk rs78574148(A;A)
Alt rs78574148(A;A)
Reference rs78574148(G;G)
Significance Other
Disease ALBUMIN MALMO-95
Variation info
Gene ALB
CLNDBN ALBUMIN MALMO-95
Reversed 0
HGVS NC_000004.11:g.74272467G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000019892.2,


[PMID 1518850OA-icon.png] Alloalbuminemia in Sweden: structural study and phenotypic distribution of nine albumin variants.


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


[PMID 15680241] Effect of genetic variation on the thermal stability of human serum albumin.