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rs77656691

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in complete genomics
Make rs77656691(G;T)
Make rs77656691(T;T)
ReferenceGRCh38 38.1/141
Chromosome4
Position73409474
GeneALB
is asnp
is mentioned by
dbSNPrs77656691
ClinGenrs77656691
ebirs77656691
HLIrs77656691
Exacrs77656691
Varsomers77656691
Maprs77656691
PheGenIrs77656691
hapmaprs77656691
1000 genomesrs77656691
hgdprs77656691
ensemblrs77656691
gopubmedrs77656691
geneviewrs77656691
scholarrs77656691
googlers77656691
pharmgkbrs77656691
gwascentralrs77656691
openSNPrs77656691
23andMers77656691
23andMe allrs77656691
SNP Nexus

SNPshotrs77656691
SNPdbers77656691
MSV3drs77656691
GWAS Ctlgrs77656691
Max Magnitude0
OMIM103600
Desc
Variant0048
Relatedalso
ClinVar
Risk rs77656691(T;T)
Alt rs77656691(T;T)
Reference Rs77656691(G;G)
Significance Other
Disease ALBUMIN HAWKES BAY
Variation info
Gene ALB
CLNDBN ALBUMIN HAWKES BAY
Reversed 0
HGVS NC_000004.11:g.74275191G>T
CLNSRC OMIM Allelic Variant UniProtKB (protein)
CLNACC RCV000019875.1,


[PMID 8347685] Albumin Hawkes Bay; a low level variant caused by loss of a sulphydryl group at position 177.