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: rs17112190
rs17112190
1.000 0.160 10 96880089 intron variant G/A snv 0.15
CUI: C0026764
Disease: Multiple Myeloma
Multiple Myeloma
Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases; Cardiovascular Diseases 0.800 1.000 1 2013 2013
dbSNP: rs7090690
rs7090690
10 96975483 intron variant G/C snv 0.21
CUI: C0005890
Disease: Body Height
Body Height
0.700 1.000 1 2019 2019
dbSNP: rs142155451
rs142155451
1.000 0.040 10 96982676 missense variant A/G snv 1.4E-05
Generalized Thyroid Hormone Resistance
Endocrine System Diseases 0.010 1.000 1 1998 1998