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rs137853302

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs137853302(G;T)
Make rs137853302(T;T)
ReferenceGRCh38 38.1/141
Chromosome22
Position32859225
GeneSYN3, TIMP3
is asnp
is mentioned by
dbSNPrs137853302
ebirs137853302
HLIrs137853302
Exacrs137853302
Varsomers137853302
Maprs137853302
PheGenIrs137853302
hapmaprs137853302
1000 genomesrs137853302
hgdprs137853302
ensemblrs137853302
gopubmedrs137853302
geneviewrs137853302
scholarrs137853302
googlers137853302
pharmgkbrs137853302
gwascentralrs137853302
openSNPrs137853302
23andMers137853302
23andMe allrs137853302
SNP Nexus

SNPshotrs137853302
SNPdbers137853302
MSV3drs137853302
GWAS Ctlgrs137853302
Max Magnitude0
OMIM188826
Desc
Variant0005
Relatedalso
ClinVar
Risk rs137853302(T;T)
Alt rs137853302(T;T)
Reference rs137853302(G;G)
Significance Pathogenic
Disease Sorsby fundus dystrophy
Variation info
Gene SYN3 TIMP3
CLNDBN Sorsby fundus dystrophy
Reversed 0
HGVS NC_000022.10:g.33255212G>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000013517.18,