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rs75470261

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs75470261(C;T)
Make rs75470261(T;T)
ReferenceGRCh38 38.1/141
Chromosome4
Position73406657
GeneALB
is asnp
is mentioned by
dbSNPrs75470261
ebirs75470261
HLIrs75470261
Exacrs75470261
Varsomers75470261
Maprs75470261
PheGenIrs75470261
hapmaprs75470261
1000 genomesrs75470261
hgdprs75470261
ensemblrs75470261
gopubmedrs75470261
geneviewrs75470261
scholarrs75470261
googlers75470261
pharmgkbrs75470261
gwascentralrs75470261
openSNPrs75470261
23andMers75470261
23andMe allrs75470261
SNP Nexus

SNPshotrs75470261
SNPdbers75470261
MSV3drs75470261
GWAS Ctlgrs75470261
Max Magnitude0
ClinVar
Risk rs75470261(T;T)
Alt rs75470261(T;T)
Reference rs75470261(C;C)
Significance Untested
Disease Analbuminemia
Variation info
Gene ALB
CLNDBN Analbuminemia
Reversed 0
HGVS NC_000004.11:g.74272374C>T
CLNSRC ClinVar
CLNACC RCV000144398.1,


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