LAMC1, laminin subunit gamma 1, 3915

N. diseases: 57; N. variants: 17
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: rs10911205
rs10911205
1 183040142 intron variant C/A snv 0.33
CUI: C0020557
Disease: Hypertriglyceridemia
Hypertriglyceridemia
Nutritional and Metabolic Diseases 0.700 1.000 1 2017 2017
dbSNP: rs10911232
rs10911232
1 183083398 intron variant C/T snv 0.33
CUI: C0020557
Disease: Hypertriglyceridemia
Hypertriglyceridemia
Nutritional and Metabolic Diseases 0.700 1.000 1 2017 2017