Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1555525654
rs1555525654
TMEM107 ; SNORD118 ; LOC105371520
TAAGGATTATCCCACCTGACGATACAGACA 0.700 CausalMutation CLINVAR

dbSNP: rs201787275
rs201787275
TMEM107 ; SNORD118 ; LOC105371520
A 0.700 CausalMutation CLINVAR

dbSNP: rs755495846
rs755495846
TMEM107 ; SNORD118 ; LOC105371520
C 0.700 CausalMutation CLINVAR

dbSNP: rs886039783
rs886039783
TMEM107 ; SNORD118 ; LOC105371520
C 0.700 CausalMutation CLINVAR

dbSNP: rs886039784
rs886039784
TMEM107 ; SNORD118 ; LOC105371520
T 0.700 CausalMutation CLINVAR

dbSNP: rs121913530
rs121913530
KRAS
0.010 GeneticVariation BEFREE Analysis of the KRAS gene showed only a G12C variation in one large cell carcinoma (LCC) patient, whereas variants were not found in adenocarcinoma (ADC) and squamous cell carcinoma (SCC) cases. 30048458

2018
dbSNP: rs754332870
rs754332870
TP53
0.010 GeneticVariation BEFREE Analysis of the KRAS gene showed only a G12C variation in one large cell carcinoma (LCC) patient, whereas variants were not found in adenocarcinoma (ADC) and squamous cell carcinoma (SCC) cases. 30048458

2018
dbSNP: rs765660823
rs765660823
DDR2
0.010 GeneticVariation BEFREE The Q808H variation in the DDR2 gene was detected in one SCC sample, while no variant was seen in the ADC and LCC subtypes. 30048458

2018