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rs137853301

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs137853301(G;T)
Make rs137853301(T;T)
ReferenceGRCh38 38.1/141
Chromosome22
Position32859306
GeneSYN3, TIMP3
is asnp
is mentioned by
dbSNPrs137853301
ebirs137853301
HLIrs137853301
Exacrs137853301
Varsomers137853301
Maprs137853301
PheGenIrs137853301
hapmaprs137853301
1000 genomesrs137853301
hgdprs137853301
ensemblrs137853301
gopubmedrs137853301
geneviewrs137853301
scholarrs137853301
googlers137853301
pharmgkbrs137853301
gwascentralrs137853301
openSNPrs137853301
23andMers137853301
23andMe allrs137853301
SNP Nexus

SNPshotrs137853301
SNPdbers137853301
MSV3drs137853301
GWAS Ctlgrs137853301
Max Magnitude0
OMIM188826
Desc
Variant0004
Relatedalso
ClinVar
Risk rs137853301(T;T)
Alt rs137853301(T;T)
Reference rs137853301(G;G)
Significance Pathogenic
Disease Sorsby fundus dystrophy
Variation info
Gene SYN3 TIMP3
CLNDBN Sorsby fundus dystrophy
Reversed 0
HGVS NC_000022.10:g.33255293G>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000013516.23,