Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1555122928
rs1555122928
T 0.700 GeneticVariation CLINVAR

dbSNP: rs1565623093
rs1565623093
0.700 CausalMutation CLINVAR

dbSNP: rs1565623439
rs1565623439
C 0.700 GeneticVariation CLINVAR

dbSNP: rs1565623713
rs1565623713
GA 0.700 GeneticVariation CLINVAR

dbSNP: rs1565626367
rs1565626367
TGATA 0.700 GeneticVariation CLINVAR

dbSNP: rs1565627110
rs1565627110
A 0.700 CausalMutation CLINVAR

dbSNP: rs1565627145
rs1565627145
GC 0.700 GeneticVariation CLINVAR

dbSNP: rs1565628520
rs1565628520
TTGCTCACCTGGTAGGCCGGCTCCAGCTTC 0.700 GeneticVariation CLINVAR

dbSNP: rs1565631430
rs1565631430
C 0.700 GeneticVariation CLINVAR

dbSNP: rs367947846
rs367947846
C 0.700 CausalMutation CLINVAR

dbSNP: rs368121566
rs368121566
T 0.700 CausalMutation CLINVAR

dbSNP: rs397515889
rs397515889
TG 0.700 GeneticVariation CLINVAR

dbSNP: rs397515903
rs397515903
G 0.700 CausalMutation CLINVAR

dbSNP: rs397515905
rs397515905
A 0.700 GeneticVariation CLINVAR

dbSNP: rs397515934
rs397515934
C 0.700 CausalMutation CLINVAR

dbSNP: rs397515960
rs397515960
AC 0.700 CausalMutation CLINVAR

dbSNP: rs397515973
rs397515973
A 0.700 CausalMutation CLINVAR

dbSNP: rs397516028
rs397516028
G 0.700 GeneticVariation CLINVAR

dbSNP: rs397516029
rs397516029
T 0.700 CausalMutation CLINVAR

dbSNP: rs397516049
rs397516049
GT 0.700 CausalMutation CLINVAR

dbSNP: rs397516059
rs397516059
CA 0.700 CausalMutation CLINVAR

dbSNP: rs397516077
rs397516077
T 0.700 GeneticVariation CLINVAR

dbSNP: rs727503166
rs727503166
C 0.700 GeneticVariation CLINVAR

dbSNP: rs727503172
rs727503172
G 0.700 CausalMutation CLINVAR

dbSNP: rs727503203
rs727503203
AG 0.700 CausalMutation CLINVAR