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

rs76454301

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs76454301(A;A)
Make rs76454301(A;G)
ReferenceGRCh38 38.1/141
Chromosome4
Position73411996
GeneALB
is asnp
is mentioned by
dbSNPrs76454301
ebirs76454301
HLIrs76454301
Exacrs76454301
Varsomers76454301
Maprs76454301
PheGenIrs76454301
hapmaprs76454301
1000 genomesrs76454301
hgdprs76454301
ensemblrs76454301
gopubmedrs76454301
geneviewrs76454301
scholarrs76454301
googlers76454301
pharmgkbrs76454301
gwascentralrs76454301
openSNPrs76454301
23andMers76454301
23andMe allrs76454301
SNP Nexus

SNPshotrs76454301
SNPdbers76454301
MSV3drs76454301
GWAS Ctlgrs76454301
Max Magnitude0
ClinVar
Risk rs76454301(A,C;A,C)
Alt rs76454301(A,C;A,C)
Reference rs76454301(G;G)
Significance Untested
Disease Analbuminemia
Variation info
Gene ALB
CLNDBN Analbuminemia
Reversed 0
HGVS NC_000004.11:g.74277713G>A
CLNSRC ClinVar
CLNACC RCV000144407.1,


[PMID 7937781OA-icon.png] Analbuminemia: three cases resulting from different point mutations in the albumin gene.