Rs121908056

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Orientationminus
Geno Mag Summary
(CTC;CTC) 0 common in complete genomics
(TCC;TCC) 0 common in clinvar
Make rs121908056(-;-)
Make rs121908056(-;CTC)
ReferenceGRCh38 38.1/141
Chromosome16
Position67940255
GeneLCAT
is asnp
is mentioned by
dbSNPrs121908056
Exacrs121908056
PheGenIrs121908056
nextbiors121908056
hapmaprs121908056
1000 genomesrs121908056
hgdprs121908056
ensemblrs121908056
gopubmedrs121908056
geneviewrs121908056
scholarrs121908056
googlers121908056
pharmgkbrs121908056
gwascentralrs121908056
openSNPrs121908056
23andMers121908056
23andMe allrs121908056
SNP Nexus

SNPshotrs121908056
SNPdbers121908056
MSV3drs121908056
Max Magnitude0
OMIM606967
Desc
Variant0017
Relatedalso
ClinVar
Risk rs121908056(;)
Alt rs121908056(;)
Reference rs121908056(TCC;TCC)
Significance Pathogenic
Disease Fish-eye disease
Variation info
Gene LCAT
CLNDBN Fish-eye disease
Reversed 1
HGVS NC_000016.9:g.67974158_67974160delGAG
CLNSRC OMIM Allelic Variant
CLNACC RCV000003857.1,