Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs6904757
rs6904757
Entrez Id: 23345
Gene Symbol: SYNE1
SYNE1
CUI: C0042834
Disease:
Vital capacity 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs35569312
rs35569312
Entrez Id: 23345
Gene Symbol: SYNE1
SYNE1
CUI: C0042133
Disease:
Uterine Fibroids 		T 0.700 GeneticVariation GWASCAT Variants associating with uterine leiomyoma highlight genetic background shared by various cancers and hormone-related traits. 30194396 2018
dbSNP: rs58415480
rs58415480
Entrez Id: 23345
Gene Symbol: SYNE1
SYNE1
CUI: C0042133
Disease:
Uterine Fibroids 		C 0.700 GeneticVariation GWASCAT Genome-wide association and epidemiological analyses reveal common genetic origins between uterine leiomyomata and endometriosis. 31649266 2019
dbSNP: rs58415480
rs58415480
Entrez Id: 23345
Gene Symbol: SYNE1
SYNE1
CUI: C0042133
Disease:
Uterine Fibroids 		G 0.700 GeneticVariation GWASCAT A Trans-Ethnic Genome-Wide Association Study of Uterine Fibroids. 31249589 2019
dbSNP: rs58415480
rs58415480
Entrez Id: 23345
Gene Symbol: SYNE1
SYNE1
CUI: C0042133
Disease:
Uterine Fibroids 		G 0.700 GeneticVariation GWASCAT Variants associating with uterine leiomyoma highlight genetic background shared by various cancers and hormone-related traits. 30194396 2018
dbSNP: rs6901631
rs6901631
Entrez Id: 23345
Gene Symbol: SYNE1
SYNE1
CUI: C0042133
Disease:
Uterine Fibroids 		T 0.700 GeneticVariation GWASCAT Genome-wide association and epidemiological analyses reveal common genetic origins between uterine leiomyomata and endometriosis. 31649266 2019
dbSNP: rs71575922
rs71575922
Entrez Id: 23345
Gene Symbol: SYNE1
SYNE1
CUI: C0042133
Disease:
Uterine Fibroids 		G 0.700 GeneticVariation GWASCAT Variants associating with uterine leiomyoma highlight genetic background shared by various cancers and hormone-related traits. 30194396 2018
dbSNP: rs119103243
rs119103243
Entrez Id: 23345;100505475
Gene Symbol: SYNE1;SYNE1-AS1
SYNE1;SYNE1-AS1
CUI: C1853116
Disease:
SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 8 (disorder) 		A 0.700 CausalMutation CLINVAR
dbSNP: rs119103244
rs119103244
Entrez Id: 23345
Gene Symbol: SYNE1
SYNE1
CUI: C1853116
Disease:
SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 8 (disorder) 		A 0.700 CausalMutation CLINVAR
dbSNP: rs119103245
rs119103245
Entrez Id: 23345
Gene Symbol: SYNE1
SYNE1
CUI: C1853116
Disease:
SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 8 (disorder) 		A 0.700 CausalMutation CLINVAR
dbSNP: rs1203553546
rs1203553546
Entrez Id: 23345
Gene Symbol: SYNE1
SYNE1
CUI: C1853116
Disease:
SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 8 (disorder) 		A 0.700 CausalMutation CLINVAR
dbSNP: rs1554226673
rs1554226673
Entrez Id: 23345
Gene Symbol: SYNE1
SYNE1
CUI: C1853116
Disease:
SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 8 (disorder) 		T 0.700 CausalMutation CLINVAR
dbSNP: rs1554247806
rs1554247806
Entrez Id: 23345
Gene Symbol: SYNE1
SYNE1
CUI: C1853116
Disease:
SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 8 (disorder) 		C 0.700 CausalMutation CLINVAR
dbSNP: rs1554553667
rs1554553667
Entrez Id: 23345
Gene Symbol: SYNE1
SYNE1
CUI: C1853116
Disease:
SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 8 (disorder) 		GT 0.700 CausalMutation CLINVAR
dbSNP: rs1554573328
rs1554573328
Entrez Id: 23345
Gene Symbol: SYNE1
SYNE1
CUI: C1853116
Disease:
SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 8 (disorder) 		A 0.700 CausalMutation CLINVAR
dbSNP: rs1554676394
rs1554676394
Entrez Id: 23345
Gene Symbol: SYNE1
SYNE1
CUI: C1853116
Disease:
SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 8 (disorder) 		A 0.700 CausalMutation CLINVAR
dbSNP: rs1554721227
rs1554721227
Entrez Id: 23345
Gene Symbol: SYNE1
SYNE1
CUI: C1853116
Disease:
SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 8 (disorder) 		A 0.700 CausalMutation CLINVAR
dbSNP: rs1554753528
rs1554753528
Entrez Id: 23345
Gene Symbol: SYNE1
SYNE1
CUI: C1853116
Disease:
SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 8 (disorder) 		C 0.700 GeneticVariation CLINVAR
dbSNP: rs1554768245
rs1554768245
Entrez Id: 23345
Gene Symbol: SYNE1
SYNE1
CUI: C1853116
Disease:
SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 8 (disorder) 		T 0.700 CausalMutation CLINVAR
dbSNP: rs1554829141
rs1554829141
Entrez Id: 23345
Gene Symbol: SYNE1
SYNE1
CUI: C1853116
Disease:
SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 8 (disorder) 		C 0.700 CausalMutation CLINVAR
dbSNP: rs1562842409
rs1562842409
Entrez Id: 23345
Gene Symbol: SYNE1
SYNE1
CUI: C1853116
Disease:
SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 8 (disorder) 		A 0.700 CausalMutation CLINVAR
dbSNP: rs1563130387
rs1563130387
Entrez Id: 23345
Gene Symbol: SYNE1
SYNE1
CUI: C1853116
Disease:
SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 8 (disorder) 		C 0.700 CausalMutation CLINVAR SYNE1 related cerebellar ataxia presents with variable phenotypes in a consanguineous family from Turkey. 28687974 2017
dbSNP: rs1563941569
rs1563941569
Entrez Id: 23345
Gene Symbol: SYNE1
SYNE1
CUI: C1853116
Disease:
SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 8 (disorder) 		A 0.700 CausalMutation CLINVAR
dbSNP: rs1564136499
rs1564136499
Entrez Id: 23345
Gene Symbol: SYNE1
SYNE1
CUI: C1853116
Disease:
SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 8 (disorder) 		T 0.700 CausalMutation CLINVAR
dbSNP: rs1564367104
rs1564367104
Entrez Id: 23345
Gene Symbol: SYNE1
SYNE1
CUI: C1853116
Disease:
SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 8 (disorder) 		A 0.700 CausalMutation CLINVAR SYNE1 mutations in autosomal recessive cerebellar ataxia. 23959263 2013