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rs78166690

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in complete genomics
Make rs78166690(A;G)
Make rs78166690(G;G)
ReferenceGRCh38 38.1/141
Chromosome4
Position73415162
GeneALB
is asnp
is mentioned by
dbSNPrs78166690
ebirs78166690
HLIrs78166690
Exacrs78166690
Varsomers78166690
Maprs78166690
PheGenIrs78166690
hapmaprs78166690
1000 genomesrs78166690
hgdprs78166690
ensemblrs78166690
gopubmedrs78166690
geneviewrs78166690
scholarrs78166690
googlers78166690
pharmgkbrs78166690
gwascentralrs78166690
openSNPrs78166690
23andMers78166690
23andMe allrs78166690
SNP Nexus

SNPshotrs78166690
SNPdbers78166690
MSV3drs78166690
GWAS Ctlgrs78166690
Max Magnitude0
OMIM103600
Desc
Variant0015
Relatedalso
ClinVar
Risk rs78166690(G;G)
Alt rs78166690(G;G)
Reference rs78166690(A;A)
Significance Other
Disease ALBUMIN MERSIN ALBUMIN NASKAPI
Variation info
Gene ALB
CLNDBN ALBUMIN MERSIN ALBUMIN NASKAPI
Reversed 0
HGVS NC_000004.11:g.74280879A>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000019843.1, RCV000019844.1,


[PMID 6933567OA-icon.png] Albumin Naskapi variant in North American Indians and Eti Turks.