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rs80358226

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs80358226(G;G)
Make rs80358226(G;T)
ReferenceGRCh38 38.1/141
Chromosome1
Position58577155
GeneTACSTD2
is asnp
is mentioned by
dbSNPrs80358226
ebirs80358226
HLIrs80358226
Exacrs80358226
Varsomers80358226
Maprs80358226
PheGenIrs80358226
hapmaprs80358226
1000 genomesrs80358226
hgdprs80358226
ensemblrs80358226
gopubmedrs80358226
geneviewrs80358226
scholarrs80358226
googlers80358226
pharmgkbrs80358226
gwascentralrs80358226
openSNPrs80358226
23andMers80358226
23andMe allrs80358226
SNP Nexus

SNPshotrs80358226
SNPdbers80358226
MSV3drs80358226
GWAS Ctlgrs80358226
Max Magnitude0
OMIM137290
Desc
Variant0005
Relatedalso
ClinVar
Risk rs80358226(G;G)
Alt rs80358226(G;G)
Reference rs80358226(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.59042827A>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000017570.27,