Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs12980275
rs12980275 		0.010 GeneticVariation BEFREE Both rs12980275 and rs8099917 were associated with an increased risk of Kaposi's sarcoma (cumulative incidence 15 versus 10%, P = 0.01 and 16 versus 10%, P = 0.009, respectively). 30234607

2018
dbSNP: rs8099917
rs8099917 		0.010 GeneticVariation BEFREE Both rs12980275 and rs8099917 were associated with an increased risk of Kaposi's sarcoma (cumulative incidence 15 versus 10%, P = 0.01 and 16 versus 10%, P = 0.009, respectively). 30234607

2018
dbSNP: rs1300339524
rs1300339524
SEMA7A
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: rs1458235863
rs1458235863
FGFR1
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: rs147436181
rs147436181
SEMA3A
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
SEMA7A
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: rs747333248
rs747333248
FGFR1
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: rs751918319
rs751918319
ANOS1
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: rs755580322
rs755580322
FGFR1
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: rs775445657
rs775445657
FGFR1
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: rs776572648
rs776572648
SEMA7A ; MIR6881
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: rs778861510
rs778861510
FGFR1
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: rs780153672
rs780153672
FGFR1
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: rs886042254
rs886042254
FGFR1
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: rs886039523
rs886039523
CHD7
0.010 GeneticVariation BEFREE In addition, both of the KS patients had a mutation in CHD7 (p.Q51X) or FGFR1 (c.91+2T>A). 22724017

2012