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rs76593094

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in complete genomics
Make rs76593094(A;A)
Make rs76593094(A;G)
ReferenceGRCh38 38.1/141
Chromosome4
Position73415108
GeneALB
is asnp
is mentioned by
dbSNPrs76593094
ebirs76593094
HLIrs76593094
Exacrs76593094
Varsomers76593094
Maprs76593094
PheGenIrs76593094
hapmaprs76593094
1000 genomesrs76593094
hgdprs76593094
ensemblrs76593094
gopubmedrs76593094
geneviewrs76593094
scholarrs76593094
googlers76593094
pharmgkbrs76593094
gwascentralrs76593094
openSNPrs76593094
23andMers76593094
23andMe allrs76593094
SNP Nexus

SNPshotrs76593094
SNPdbers76593094
MSV3drs76593094
GWAS Ctlgrs76593094
Max Magnitude0
OMIM103600
Desc
Variant0012
Relatedalso
ClinVar
Risk rs76593094(A;A)
Alt rs76593094(A;A)
Reference rs76593094(G;G)
Significance Other
Disease ALBUMIN HIROSHIMA 1
Variation info
Gene ALB
CLNDBN ALBUMIN HIROSHIMA 1
Reversed 0
HGVS NC_000004.11:g.74280825G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000019839.1,


[PMID 2762316OA-icon.png] Point substitutions in Japanese alloalbumins.