Source: GWASCAT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs12035735
rs12035735
LRRC8D
1 89839786 intron variant G/A snv 1.4E-03
CUI: C0021831
Disease: Intestinal Diseases
Intestinal Diseases 		0.700 1.000 1 2018 2018
dbSNP: rs12035735
rs12035735
LRRC8D
1 89839786 intron variant G/A snv 1.4E-03
CUI: C0017178
Disease: Gastrointestinal Diseases
Gastrointestinal Diseases 		0.700 1.000 1 2018 2018
dbSNP: rs12035735
rs12035735
LRRC8D
1 89839786 intron variant G/A snv 1.4E-03
CUI: C0012242
Disease: Digestive System Disorders
Digestive System Disorders 		0.700 1.000 1 2018 2018
dbSNP: rs12035735
rs12035735
LRRC8D
1 89839786 intron variant G/A snv 1.4E-03
CUI: C0021390
Disease: Inflammatory Bowel Diseases
Inflammatory Bowel Diseases 		0.700 1.000 1 2018 2018
dbSNP: rs78359677
rs78359677
LRRC8D
1.000 0.080 1 89907211 intron variant A/C;G;T snv
CUI: C0149782
Disease: Squamous cell carcinoma of lung
Squamous cell carcinoma of lung 		0.700 1.000 1 2017 2017