Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs886040975
rs886040975
C1S
0.800 GeneticVariation UNIPROT Periodontal Ehlers-Danlos Syndrome Is Caused by Mutations in C1R and C1S, which Encode Subcomponents C1r and C1s of Complement. 27745832

2016
dbSNP: rs886040975
rs886040975
C1S
C 0.800 CausalMutation CLINVAR

dbSNP: rs886040975
rs886040975
C1S
C 0.800 GeneticVariation CLINVAR

dbSNP: rs1057515579
rs1057515579
C1R
G 0.700 GeneticVariation CLINVAR

dbSNP: rs1057518643
rs1057518643
C1R
C 0.700 GeneticVariation CLINVAR

dbSNP: rs1057518645
rs1057518645
C1R
A 0.700 GeneticVariation CLINVAR

dbSNP: rs1057518646
rs1057518646
C1R
TGTCC 0.700 GeneticVariation CLINVAR

dbSNP: rs1057519025
rs1057519025
C1R ; C1RL
AT 0.700 GeneticVariation CLINVAR

dbSNP: rs1057519026
rs1057519026
C1R
T 0.700 GeneticVariation CLINVAR

dbSNP: rs1057519576
rs1057519576
C1R
C 0.700 GeneticVariation CLINVAR

dbSNP: rs1057519577
rs1057519577
C1R
G 0.700 GeneticVariation CLINVAR

dbSNP: rs1057519578
rs1057519578
C1R
G 0.700 GeneticVariation CLINVAR

dbSNP: rs1057519579
rs1057519579
C1R
C 0.700 GeneticVariation CLINVAR

dbSNP: rs1057519580
rs1057519580
C1R
TATTACATGA 0.700 GeneticVariation CLINVAR

dbSNP: rs1060499554
rs1060499554
C1R
G 0.700 GeneticVariation CLINVAR

dbSNP: rs760277934
rs760277934
C1R
G 0.700 GeneticVariation CLINVAR

dbSNP: rs769707492
rs769707492
C1R
C 0.700 GeneticVariation CLINVAR

dbSNP: rs886040974
rs886040974
C1S
A 0.700 CausalMutation CLINVAR

dbSNP: rs886040974
rs886040974
C1S
A 0.700 GeneticVariation CLINVAR