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Rs121908057

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Orientationminus
is asnp
is mentioned by
dbSNPrs121908057
PheGenIrs121908057
nextbiors121908057
hapmaprs121908057
1000 genomesrs121908057
hgdprs121908057
ensemblrs121908057
gopubmedrs121908057
geneviewrs121908057
scholarrs121908057
googlers121908057
pharmgkbrs121908057
gwascentralrs121908057
openSNPrs121908057
23andMers121908057
23andMe allrs121908057
SNP Nexus

SNPshotrs121908057
SNPdbers121908057
MSV3drs121908057
GeneLCAT
Chromosome16
Orientationminus
Position67942731
ReferenceGRCh38 38.1/141
Max Magnitude0
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs121908057(A;G)
Make rs121908057(G;G)
OMIM606967
Desc
Variant0018
Relatedalso
ClinVar
Risk rs121908057(G;G)
Alt rs121908057(G;G)
Reference rs121908057(A;A)
Significance 5
Disease Fish-eye disease
ClinVar info
Gene LCAT
CLNDBN Fish-eye disease
Reversed 1
CLNHGVS NC_000016.9:g.67976634T>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000003858.1