Have questions? Visit https://www.reddit.com/r/SNPedia

rs80358227

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs80358227(A;T)
Make rs80358227(T;T)
ReferenceGRCh38 38.1/141
Chromosome1
Position58576802
GeneTACSTD2
is asnp
is mentioned by
dbSNPrs80358227
ebirs80358227
HLIrs80358227
Exacrs80358227
Varsomers80358227
Maprs80358227
PheGenIrs80358227
hapmaprs80358227
1000 genomesrs80358227
hgdprs80358227
ensemblrs80358227
gopubmedrs80358227
geneviewrs80358227
scholarrs80358227
googlers80358227
pharmgkbrs80358227
gwascentralrs80358227
openSNPrs80358227
23andMers80358227
23andMe allrs80358227
SNP Nexus

SNPshotrs80358227
SNPdbers80358227
MSV3drs80358227
GWAS Ctlgrs80358227
Max Magnitude0
OMIM137290
Desc
Variant0006
Relatedalso
ClinVar
Risk rs80358227(T;T)
Alt rs80358227(T;T)
Reference rs80358227(A;A)
Significance Pathogenic
Disease Lattice corneal dystrophy Type III
Variation info
Gene TACSTD2
CLNDBN Lattice corneal dystrophy Type III
Reversed 0
HGVS NC_000001.10:g.59042474A>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000017571.23,