Source: ALL

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: rs12444795
rs12444795
GLYR1
16 4840065 non coding transcript exon variant C/T snv 0.13
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms 		0.700 1.000 1 2017 2017
dbSNP: rs2075466
rs2075466
GLYR1
16 4822969 intron variant G/A;C snv 4.0E-06; 0.30
CUI: C1305855
Disease: Body mass index
Body mass index 		0.700 1.000 1 2019 2019
dbSNP: rs4619406
rs4619406
GLYR1
16 4829765 intron variant T/C snv 0.58
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2019 2019
dbSNP: rs8064024
rs8064024
GLYR1
16 4805278 synonymous variant A/G snv 0.52 0.57
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms 		0.700 1.000 1 2017 2017