RAB3IL1, RAB3A interacting protein like 1, 5866

N. diseases: 5; N. variants: 40
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: rs174478
rs174478
11 61911104 intron variant T/G snv 0.31
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
0.700 1.000 1 2012 2012
dbSNP: rs174479
rs174479
11 61911282 intron variant C/G snv 0.17
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
0.700 1.000 1 2012 2012
dbSNP: rs17764935
rs17764935
11 61897285 downstream gene variant G/A snv 4.9E-02
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
0.700 1.000 1 2012 2012
dbSNP: rs2158026
rs2158026
11 61926922 regulatory region variant C/T snv 0.49
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
0.700 1.000 1 2012 2012
dbSNP: rs2521562
rs2521562
11 61924547 upstream gene variant C/A;G;T snv
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
0.700 1.000 1 2012 2012
dbSNP: rs2521564
rs2521564
11 61928862 regulatory region variant G/A snv 0.48
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
0.700 1.000 1 2012 2012
dbSNP: rs2521565
rs2521565
11 61929203 intergenic variant A/G snv 0.51
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
0.700 1.000 1 2012 2012
dbSNP: rs2521566
rs2521566
11 61929413 intergenic variant A/G snv 0.52
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
0.700 1.000 1 2012 2012
dbSNP: rs2521567
rs2521567
11 61931583 intergenic variant G/A snv 0.48
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
0.700 1.000 1 2012 2012
dbSNP: rs2521568
rs2521568
11 61933461 upstream gene variant G/C snv 9.5E-02
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
0.700 1.000 1 2012 2012
dbSNP: rs2521569
rs2521569
11 61933946 upstream gene variant G/A snv 9.9E-02
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
0.700 1.000 1 2012 2012
dbSNP: rs2524292
rs2524292
11 61927674 regulatory region variant T/G snv 9.7E-02
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
0.700 1.000 1 2012 2012
dbSNP: rs2524293
rs2524293
11 61943066 intergenic variant A/C snv 0.48
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
0.700 1.000 1 2012 2012
dbSNP: rs2727261
rs2727261
11 61944659 regulatory region variant T/C;G snv
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
0.700 1.000 1 2012 2012
dbSNP: rs2727266
rs2727266
11 61936862 upstream gene variant A/G snv 9.8E-02
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
0.700 1.000 1 2012 2012
dbSNP: rs2727267
rs2727267
11 61938644 downstream gene variant G/A snv 9.5E-02
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
0.700 1.000 1 2012 2012
dbSNP: rs2727273
rs2727273
11 61935131 upstream gene variant C/A;T snv
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
0.700 1.000 1 2012 2012
dbSNP: rs2736598
rs2736598
11 61938663 downstream gene variant T/A;C snv
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
0.700 1.000 1 2012 2012
dbSNP: rs2736600
rs2736600
11 61938539 downstream gene variant T/A;C snv
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
0.700 1.000 1 2012 2012
dbSNP: rs2736601
rs2736601
11 61938049 downstream gene variant C/T snv 9.5E-02
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
0.700 1.000 1 2012 2012
dbSNP: rs2736603
rs2736603
11 61937877 upstream gene variant A/T snv 0.46
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
0.700 1.000 1 2012 2012
dbSNP: rs2736604
rs2736604
11 61932355 intergenic variant C/A snv 9.8E-02
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
0.700 1.000 1 2012 2012
dbSNP: rs741888
rs741888
11 61923072 upstream gene variant C/A;G;T snv
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
0.700 1.000 1 2012 2012
dbSNP: rs882169
rs882169
11 61924658 upstream gene variant T/C snv 0.50
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
0.700 1.000 1 2012 2012
dbSNP: rs2736600
rs2736600
11 61938539 downstream gene variant T/A;C snv
CUI: C0042834
Disease: Vital capacity
Vital capacity
0.700 1.000 1 2019 2019