Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs28362930
rs28362930
Entrez Id: 8482
Gene Symbol: SEMA7A
SEMA7A
CUI: C0024141
Disease:
Lupus Erythematosus, Systemic 		0.010 GeneticVariation BEFREE The allele frequency of G (rs28362930) was higher in S</span>LE patients with renal disorder. 31394943 2019
dbSNP: rs28362930
rs28362930
Entrez Id: 8482
Gene Symbol: SEMA7A
SEMA7A
CUI: C0022658
Disease:
Kidney Diseases 		0.010 GeneticVariation BEFREE The allele frequency of G (rs28362930) was higher in SLE patients with renal disorder. 31394943 2019
dbSNP: rs28362930
rs28362930
Entrez Id: 8482
Gene Symbol: SEMA7A
SEMA7A
CUI: C0014060
Disease:
Encephalitis, St. Louis 		0.010 GeneticVariation BEFREE The allele frequency of G (rs28362930) was higher in S</span>LE patients with renal disorder. 31394943 2019
dbSNP: rs741761
rs741761
Entrez Id: 8482;102465530
Gene Symbol: SEMA7A;MIR6881
SEMA7A;MIR6881
CUI: C0014060
Disease:
Encephalitis, St. Louis 		0.010 GeneticVariation BEFREE There were differences in the genotype frequencies and allele frequencies of rs741761 between SLE patients with and without arthritis. 31394943 2019
dbSNP: rs741761
rs741761
Entrez Id: 8482;102465530
Gene Symbol: SEMA7A;MIR6881
SEMA7A;MIR6881
CUI: C0024141
Disease:
Lupus Erythematosus, Systemic 		0.010 GeneticVariation BEFREE There were differences in the genotype frequencies and allele frequencies of rs741761 between SLE patients with and without arthritis. 31394943 2019
dbSNP: rs741761
rs741761
Entrez Id: 8482;102465530
Gene Symbol: SEMA7A;MIR6881
SEMA7A;MIR6881
CUI: C0003864
Disease:
Arthritis 		0.010 GeneticVariation BEFREE There were differences in the genotype frequencies and allele frequencies of rs741761 between SLE patients with and without arthritis. 31394943 2019
dbSNP: rs1300339524
rs1300339524
Entrez Id: 8482
Gene Symbol: SEMA7A
SEMA7A
CUI: C0036220
Disease:
Kaposi Sarcoma 		0.010 GeneticVariation BEFREE Three heterozygous variants (c.458A>G (p.Asn153Ser), c.1253A>G (p.Asn418Ser), and c.1303G>A (p.Val435Ile)) were found in SEMA3A in three KS patients, two of which also had a mutation in FGFR1. 24522099 2014
dbSNP: rs200895370
rs200895370
Entrez Id: 8482
Gene Symbol: SEMA7A
SEMA7A
CUI: C3899503
Disease:
Congenital hypogonadotropic hypogonadism 		0.010 GeneticVariation BEFREE Two rare heterozygous variants (c.442C>T (p.Arg148Trp) and c.1421G>A (p.Arg474Gln)) in SEMA7A were found in one male nHH patient with a previously identified KISS1R nonsense variant and one male KS patient with a previously identified mutation in KAL1, respectively. 24522099 2014
dbSNP: rs200895370
rs200895370
Entrez Id: 8482
Gene Symbol: SEMA7A
SEMA7A
CUI: C0036220
Disease:
Kaposi Sarcoma 		0.010 GeneticVariation BEFREE Two rare heterozygous variants (c.442C>T (p.Arg148Trp) and c.1421G>A (p.Arg474Gln)) in SEMA7A were found in one male nHH patient with a previously identified KISS1R nonsense variant and one male KS patient with a previously identified mutation in KAL1, respectively. 24522099 2014
dbSNP: rs776572648
rs776572648
Entrez Id: 8482;102465530
Gene Symbol: SEMA7A;MIR6881
SEMA7A;MIR6881
CUI: C3899503
Disease:
Congenital hypogonadotropic hypogonadism 		0.010 GeneticVariation BEFREE Two rare heterozygous variants (c.442C>T (p.Arg148Trp) and c.1421G>A (p.Arg474Gln)) in SEMA7A were found in one male nHH patient with a previously identified KISS1R nonsense variant and one male KS patient with a previously identified mutation in KAL1, respectively. 24522099 2014
dbSNP: rs776572648
rs776572648
Entrez Id: 8482;102465530
Gene Symbol: SEMA7A;MIR6881
SEMA7A;MIR6881
CUI: C0036220
Disease:
Kaposi Sarcoma 		0.010 GeneticVariation BEFREE Two rare heterozygous variants (c.442C>T (p.Arg148Trp) and c.1421G>A (p.Arg474Gln)) in SEMA7A were found in one male nHH patient with a previously identified KISS1R nonsense variant and one male KS patient with a previously identified mutation in KAL1, respectively. 24522099 2014