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rs137853298

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs137853298(A;T)
Make rs137853298(T;T)
ReferenceGRCh38 38.1/141
Chromosome22
Position32859351
GeneSYN3, TIMP3
is asnp
is mentioned by
dbSNPrs137853298
ebirs137853298
HLIrs137853298
Exacrs137853298
Varsomers137853298
Maprs137853298
PheGenIrs137853298
hapmaprs137853298
1000 genomesrs137853298
hgdprs137853298
ensemblrs137853298
gopubmedrs137853298
geneviewrs137853298
scholarrs137853298
googlers137853298
pharmgkbrs137853298
gwascentralrs137853298
openSNPrs137853298
23andMers137853298
23andMe allrs137853298
SNP Nexus

SNPshotrs137853298
SNPdbers137853298
MSV3drs137853298
GWAS Ctlgrs137853298
Max Magnitude0
OMIM188826
Desc
Variant0001
Relatedalso
ClinVar
Risk rs137853298(T;T)
Alt rs137853298(T;T)
Reference rs137853298(A;A)
Significance Pathogenic
Disease Sorsby fundus dystrophy
Variation info
Gene SYN3 TIMP3
CLNDBN Sorsby fundus dystrophy
Reversed 0
HGVS NC_000022.10:g.33255338A>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000013513.25,