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rs397515467

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs397515467(G;T)
Make rs397515467(T;T)
ReferenceGRCh38 38.1/141
Chromosome16
Position77322434
GeneADAMTS18
is asnp
is mentioned by
dbSNPrs397515467
ebirs397515467
HLIrs397515467
Exacrs397515467
Varsomers397515467
Maprs397515467
PheGenIrs397515467
hapmaprs397515467
1000 genomesrs397515467
hgdprs397515467
ensemblrs397515467
gopubmedrs397515467
geneviewrs397515467
scholarrs397515467
googlers397515467
pharmgkbrs397515467
gwascentralrs397515467
openSNPrs397515467
23andMers397515467
23andMe allrs397515467
SNP Nexus

SNPshotrs397515467
SNPdbers397515467
MSV3drs397515467
GWAS Ctlgrs397515467
Max Magnitude0
ClinVar
Risk rs397515467(A,T;A,T)
Alt rs397515467(A,T;A,T)
Reference rs397515467(G;G)
Significance Pathogenic
Disease Microcornea
Variation info
Gene ADAMTS18
CLNDBN Microcornea, myopic chorioretinal atrophy, and telecanthus
Reversed 1
HGVS NC_000016.9:g.77356331C>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000056279.2,