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

rs76483862

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in complete genomics
Make rs76483862(A;A)
Make rs76483862(A;G)
ReferenceGRCh38 38.1/141
Chromosome4
Position73416280
GeneALB
is asnp
is mentioned by
dbSNPrs76483862
ebirs76483862
HLIrs76483862
Exacrs76483862
Varsomers76483862
Maprs76483862
PheGenIrs76483862
hapmaprs76483862
1000 genomesrs76483862
hgdprs76483862
ensemblrs76483862
gopubmedrs76483862
geneviewrs76483862
scholarrs76483862
googlers76483862
pharmgkbrs76483862
gwascentralrs76483862
openSNPrs76483862
23andMers76483862
23andMe allrs76483862
SNP Nexus

SNPshotrs76483862
SNPdbers76483862
MSV3drs76483862
GWAS Ctlgrs76483862
Max Magnitude0
OMIM103600
Desc
Variant0018
Relatedalso
ClinVar
Risk rs76483862(A;A)
Alt rs76483862(A;A)
Reference rs76483862(G;G)
Significance Other
Disease ALBUMIN HIROSHIMA 2
Variation info
Gene ALB
CLNDBN ALBUMIN HIROSHIMA 2
Reversed 0
HGVS NC_000004.11:g.74281997G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000019848.1,


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