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rs80358228

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs80358228(C;C)
Make rs80358228(C;T)
ReferenceGRCh38 38.1/141
Chromosome1
Position58576600
GeneTACSTD2
is asnp
is mentioned by
dbSNPrs80358228
ebirs80358228
HLIrs80358228
Exacrs80358228
Varsomers80358228
Maprs80358228
PheGenIrs80358228
hapmaprs80358228
1000 genomesrs80358228
hgdprs80358228
ensemblrs80358228
gopubmedrs80358228
geneviewrs80358228
scholarrs80358228
googlers80358228
pharmgkbrs80358228
gwascentralrs80358228
openSNPrs80358228
23andMers80358228
23andMe allrs80358228
SNP Nexus

SNPshotrs80358228
SNPdbers80358228
MSV3drs80358228
GWAS Ctlgrs80358228
Max Magnitude0
OMIM137290
Desc
Variant0008
Relatedalso
ClinVar
Risk rs80358228(C;C)
Alt rs80358228(C;C)
Reference rs80358228(T;T)
Significance Pathogenic
Disease Lattice corneal dystrophy Type III
Variation info
Gene TACSTD2
CLNDBN Lattice corneal dystrophy Type III
Reversed 1
HGVS NC_000001.10:g.59042272A>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000017573.27,