Have questions? Visit https://www.reddit.com/r/SNPedia

rs77050410

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in complete genomics
Make rs77050410(A;A)
Make rs77050410(A;G)
ReferenceGRCh38 38.1/141
Chromosome4
Position73406741
GeneALB
is asnp
is mentioned by
dbSNPrs77050410
ebirs77050410
HLIrs77050410
Exacrs77050410
Varsomers77050410
Maprs77050410
PheGenIrs77050410
hapmaprs77050410
1000 genomesrs77050410
hgdprs77050410
ensemblrs77050410
gopubmedrs77050410
geneviewrs77050410
scholarrs77050410
googlers77050410
pharmgkbrs77050410
gwascentralrs77050410
openSNPrs77050410
23andMers77050410
23andMe allrs77050410
SNP Nexus

SNPshotrs77050410
SNPdbers77050410
MSV3drs77050410
GWAS Ctlgrs77050410
Max Magnitude0
OMIM103600
Desc
Variant0033
Relatedalso
ClinVar
Risk rs77050410(A;A)
Alt rs77050410(A;A)
Reference rs77050410(G;G)
Significance Other
Disease ALBUMIN TORINO
Variation info
Gene ALB
CLNDBN ALBUMIN TORINO
Reversed 0
HGVS NC_000004.11:g.74272458G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000019878.1,


[PMID 2247440OA-icon.png] Mutations in genetic variants of human serum albumin found in Italy.