Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs70993900
rs70993900 		0.710 GeneticVariation GWASCAT Subtype-specific inherited predisposition to pemphigus in the Chinese population. 30230522

2019
dbSNP: rs70993900
rs70993900 		0.710 GeneticVariation BEFREE The strongest associated single-nucleotide polymorphisms are in the human leucocyte antigen (HLA) region: rs70993900 (PV; P = 1·5 × 10<sup>-45</sup> ) and rs9469220 (PF; P = 1·1 × 10<sup>-8</sup> ). 30230522

2019
dbSNP: rs9469220
rs9469220 		G 0.710 GeneticVariation GWASCAT Subtype-specific inherited predisposition to pemphigus in the Chinese population. 30230522

2019
dbSNP: rs9469220
rs9469220 		0.710 GeneticVariation BEFREE The strongest associated single-nucleotide polymorphisms are in the human leucocyte antigen (HLA) region: rs70993900 (PV; P = 1·5 × 10<sup>-45</sup> ) and rs9469220 (PF; P = 1·1 × 10<sup>-8</sup> ). 30230522

2019
dbSNP: rs11218708
rs11218708 		A 0.710 GeneticVariation GWASCAT Association Study and Fine-Mapping Major Histocompatibility Complex Analysis of Pemphigus Vulgaris in a Han Chinese Population. 29857070

2018
dbSNP: rs11218708
rs11218708 		0.710 GeneticVariation BEFREE We identified rs11218708 (P = 3.1 × 10<sup>-8</sup>, odds ratio = 1.54) at chromosome locus 11q24.1 as significantly associated with PV. 29857070

2018
dbSNP: rs7454108
rs7454108 		0.710 GeneticVariation GWASCAT Association Study and Fine-Mapping Major Histocompatibility Complex Analysis of Pemphigus Vulgaris in a Han Chinese Population. 29857070

2018
dbSNP: rs7454108
rs7454108 		0.710 GeneticVariation BEFREE A fine-mapping analysis of PV risk in the major histocompatibility complex region showed three independent variants predisposed to PV using stepwise analysis: HLA-DRB1*14:04 (P = 2.47 × 10<sup>-38</sup>, odds ratio = 6.28), rs7454108 at the TAP2 gene (P = 2.78 × 10<sup>-12</sup>, odds ratio = 3.25), and rs1051336 at the HLA-DRA gene (P = 3.06 × 10<sup>-6</sup>, odds ratio = 0.33). 29857070

2018
dbSNP: rs1074532
rs1074532 		A 0.700 GeneticVariation GWASCAT Investigation of the predisposing factor of pemphigus and its clinical subtype through a genome-wide association and next generation sequence analysis. 30169916

2019
dbSNP: rs28483633
rs28483633 		0.700 GeneticVariation GWASCAT Association Study and Fine-Mapping Major Histocompatibility Complex Analysis of Pemphigus Vulgaris in a Han Chinese Population. 29857070

2018
dbSNP: rs12660382
rs12660382
HCP5
0.700 GeneticVariation GWASDB Population-specific association between a polymorphic variant in ST18, encoding a pro-apoptotic molecule, and pemphigus vulgaris. 22437316

2012
dbSNP: rs1980495
rs1980495
TSBP1-AS1
0.700 GeneticVariation GWASDB Population-specific association between a polymorphic variant in ST18, encoding a pro-apoptotic molecule, and pemphigus vulgaris. 22437316

2012
dbSNP: rs2071286
rs2071286
NOTCH4
0.700 GeneticVariation GWASDB Population-specific association between a polymorphic variant in ST18, encoding a pro-apoptotic molecule, and pemphigus vulgaris. 22437316

2012
dbSNP: rs2244839
rs2244839
HCP5 ; HCG26
0.700 GeneticVariation GWASDB Population-specific association between a polymorphic variant in ST18, encoding a pro-apoptotic molecule, and pemphigus vulgaris. 22437316

2012
dbSNP: rs2246618
rs2246618
MICB
0.700 GeneticVariation GWASDB Population-specific association between a polymorphic variant in ST18, encoding a pro-apoptotic molecule, and pemphigus vulgaris. 22437316

2012
dbSNP: rs2395157
rs2395157
TSBP1-AS1
0.700 GeneticVariation GWASDB Population-specific association between a polymorphic variant in ST18, encoding a pro-apoptotic molecule, and pemphigus vulgaris. 22437316

2012
dbSNP: rs2395163
rs2395163 		0.700 GeneticVariation GWASDB Population-specific association between a polymorphic variant in ST18, encoding a pro-apoptotic molecule, and pemphigus vulgaris. 22437316

2012
dbSNP: rs2395488
rs2395488
HCP5
0.700 GeneticVariation GWASDB Population-specific association between a polymorphic variant in ST18, encoding a pro-apoptotic molecule, and pemphigus vulgaris. 22437316

2012
dbSNP: rs2516049
rs2516049
HLA-DRB1
0.700 GeneticVariation GWASDB Population-specific association between a polymorphic variant in ST18, encoding a pro-apoptotic molecule, and pemphigus vulgaris. 22437316

2012
dbSNP: rs2516424
rs2516424
MICB-DT
0.700 GeneticVariation GWASDB Population-specific association between a polymorphic variant in ST18, encoding a pro-apoptotic molecule, and pemphigus vulgaris. 22437316

2012
dbSNP: rs2523647
rs2523647
MICB-DT
0.700 GeneticVariation GWASDB Population-specific association between a polymorphic variant in ST18, encoding a pro-apoptotic molecule, and pemphigus vulgaris. 22437316

2012
dbSNP: rs2858331
rs2858331 		0.700 GeneticVariation GWASDB Population-specific association between a polymorphic variant in ST18, encoding a pro-apoptotic molecule, and pemphigus vulgaris. 22437316

2012
dbSNP: rs3763309
rs3763309
BTNL2 ; TSBP1-AS1
0.700 GeneticVariation GWASDB Population-specific association between a polymorphic variant in ST18, encoding a pro-apoptotic molecule, and pemphigus vulgaris. 22437316

2012
dbSNP: rs3892710
rs3892710 		0.700 GeneticVariation GWASDB Population-specific association between a polymorphic variant in ST18, encoding a pro-apoptotic molecule, and pemphigus vulgaris. 22437316

2012
dbSNP: rs3916765
rs3916765
LOC102725019
0.700 GeneticVariation GWASDB Population-specific association between a polymorphic variant in ST18, encoding a pro-apoptotic molecule, and pemphigus vulgaris. 22437316

2012