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rs78283180

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in complete genomics
Make rs78283180(A;G)
Make rs78283180(G;G)
ReferenceGRCh38 38.1/141
Chromosome4
Position73409363
GeneALB
is asnp
is mentioned by
dbSNPrs78283180
ebirs78283180
HLIrs78283180
Exacrs78283180
Varsomers78283180
Maprs78283180
PheGenIrs78283180
hapmaprs78283180
1000 genomesrs78283180
hgdprs78283180
ensemblrs78283180
gopubmedrs78283180
geneviewrs78283180
scholarrs78283180
googlers78283180
pharmgkbrs78283180
gwascentralrs78283180
openSNPrs78283180
23andMers78283180
23andMe allrs78283180
SNP Nexus

SNPshotrs78283180
SNPdbers78283180
MSV3drs78283180
GWAS Ctlgrs78283180
Max Magnitude0
OMIM103600
Desc
Variant0046
Relatedalso
ClinVar
Risk rs78283180(G;G)
Alt rs78283180(G;G)
Reference rs78283180(A;A)
Significance Other
Disease ALBUMIN ASOLA
Variation info
Gene ALB
CLNDBN ALBUMIN ASOLA
Reversed 0
HGVS NC_000004.11:g.74275080A>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000019891.1,


[PMID 7882997] A genetic variant of albumin (albumin Asola; Tyr140-->Cys) with no free -SH group but with an additional disulfide bridge.