Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1057518806
rs1057518806
HMBS
T 0.700 GeneticVariation CLINVAR

dbSNP: rs1057518886
rs1057518886
HMBS
A 0.700 CausalMutation CLINVAR

dbSNP: rs1163944538
rs1163944538
TMEM94
GA 0.700 CausalMutation CLINVAR

dbSNP: rs1352010373
rs1352010373
TMEM94
C 0.700 CausalMutation CLINVAR

dbSNP: rs148636776
rs148636776
ATXN2 ; SH2B3
A 0.700 CausalMutation CLINVAR

dbSNP: rs1553655558
rs1553655558
TRIP12
G 0.700 CausalMutation CLINVAR

dbSNP: rs1554995260
rs1554995260
SERPING1
GT 0.700 CausalMutation CLINVAR

dbSNP: rs1555206402
rs1555206402
HMBS
A 0.700 CausalMutation CLINVAR

dbSNP: rs1555738475
rs1555738475
STK11
T 0.700 CausalMutation CLINVAR

dbSNP: rs28934907
rs28934907
MECP2
A 0.700 CausalMutation CLINVAR

dbSNP: rs606231435
rs606231435
ATP1A3
T 0.700 CausalMutation CLINVAR

dbSNP: rs8133052
rs8133052
CBR3 ; CBR3-AS1
0.010 GeneticVariation BEFREE Regarding the docetaxel phase, high levels of abdominal pain and mucositis were related to CBR3 gene (rs8133052) polymorphism and diabetes respectively. 31056713

2020
dbSNP: rs28940580
rs28940580
MEFV
0.010 GeneticVariation BEFREE Their parents were heterozygous for the same mutation p.M680I, however, the mother showed severe symptoms of FMF (recurrent attacks of fever, arthralgia and arthritis, abdominal pain, thoracic pain), the father showed recurrent pustulosis prevalent on the hands and limbs, with arthralgia and abdominal pain. 31443670

2019
dbSNP: rs6795970
rs6795970
SCN10A
0.010 GeneticVariation BEFREE This is the first report linking the rs6795970 mutation with postoperative abdominal pain in humans. 31642403

2019
dbSNP: rs11466023
rs11466023
MEFV
0.010 GeneticVariation BEFREE Patients with P369S have higher abdominal pain, chest pain and fever than expected. 28483595

2017
dbSNP: rs224222
rs224222
MEFV
0.010 GeneticVariation BEFREE The frequency of abdominal pain was significantly lower in patients with homozygous R202Q alteration (p = 0.021), whereas patients with heterozygous R202Q mutations, though not statistically significant, had a higher frequency of arthralgia/myalgia (40.0 %, p = 0.05). 24718488

2014
dbSNP: rs3743930
rs3743930
MEFV
0.010 GeneticVariation BEFREE Significant increase in abdominal pain and arthritis was found in patients with homozygote M694V mutation compared to those with E148Q mutation. 19777236

2010
dbSNP: rs61752717
rs61752717
MEFV
0.010 GeneticVariation BEFREE M694V gene mutation may be associated with increased frequency of abdominal pain, arthritis and the presence of amyloidosis. 19777236

2010