SLAIN2, SLAIN motif family member 2, 57606

N. diseases: 8; N. variants: 3
Source: ALL
Variant DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Disease Class Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs6837335
rs6837335 		1.000 0.040 4 48361966 intron variant A/G snv 0.58
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		Digestive System Diseases 0.800 1.000 1 2012 2012
dbSNP: rs551980034
rs551980034 		1.000 4 48374339 intron variant C/T snv 9.8E-05
CUI: C2242776
Disease: Plexiform leiomyoma
Plexiform leiomyoma 		0.700 1.000 1 2018 2018
dbSNP: rs551980034
rs551980034 		1.000 4 48374339 intron variant C/T snv 9.8E-05
CUI: C0042133
Disease: Uterine Fibroids
Uterine Fibroids 		Neoplasms 0.700 1.000 1 2018 2018
dbSNP: rs7438704
rs7438704 		1.000 0.040 4 48361228 intron variant A/G snv 0.58
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		Digestive System Diseases 0.700 1.000 1 2015 2015
dbSNP: rs7438704
rs7438704 		1.000 0.040 4 48361228 intron variant A/G snv 0.58
CUI: C0021390
Disease: Inflammatory Bowel Diseases
Inflammatory Bowel Diseases 		Digestive System Diseases 0.700 1.000 1 2015 2015