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rs1800580

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in complete genomics
Make rs1800580(C;C)
Make rs1800580(C;G)
ReferenceGRCh38 38.1/141
Chromosome4
Position73419640
GeneALB
is asnp
is mentioned by
dbSNPrs1800580
ebirs1800580
HLIrs1800580
Exacrs1800580
Varsomers1800580
Maprs1800580
PheGenIrs1800580
hapmaprs1800580
1000 genomesrs1800580
hgdprs1800580
ensemblrs1800580
gopubmedrs1800580
geneviewrs1800580
scholarrs1800580
googlers1800580
pharmgkbrs1800580
gwascentralrs1800580
openSNPrs1800580
23andMers1800580
23andMe allrs1800580
SNP Nexus

SNPshotrs1800580
SNPdbers1800580
MSV3drs1800580
GWAS Ctlgrs1800580
Max Magnitude0
OMIM103600
Desc
Variant0038
Relatedalso


ClinVar
Risk rs1800580(C;C)
Alt rs1800580(C;C)
Reference rs1800580(G;G)
Significance Other
Disease ALBUMIN RUGBY PARK
Variation info
Gene ALB
CLNDBN ALBUMIN RUGBY PARK
Reversed 0
HGVS NC_000004.11:g.74285357G>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000019883.1,



[PMID 1390939] Albumin Rugby Park: a truncated albumin variant caused by a G-->C splice-site mutation in intron 13.

[PMID 9392528] Effect of genetic variation on the fatty acid-binding properties of human serum albumin and proalbumin.