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: 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: rs1534842
rs1534842
11 61946118 upstream gene variant A/G snv 0.28
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
0.700 1.000 1 2012 2012
dbSNP: rs174472
rs174472
11 61904484 intron variant A/G snv 0.41
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
0.700 1.000 1 2012 2012
dbSNP: rs174472
rs174472
11 61904484 intron variant A/G snv 0.41
CUI: C0202177
Disease: Phospholipid measurement
Phospholipid measurement
0.700 1.000 1 2011 2011
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: rs2727266
rs2727266
11 61936862 upstream gene variant A/G snv 9.8E-02
CUI: C0202177
Disease: Phospholipid measurement
Phospholipid measurement
0.700 1.000 1 2011 2011
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: rs2235093
rs2235093
11 61897650 3 prime UTR variant A/G;T snv
CUI: C0202177
Disease: Phospholipid measurement
Phospholipid measurement
0.700 1.000 1 2011 2011
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: rs174476
rs174476
11 61906646 synonymous variant C/A;G;T snv 0.30
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
0.700 1.000 1 2012 2012
dbSNP: rs174476
rs174476
11 61906646 synonymous variant C/A;G;T snv 0.30
CUI: C0202177
Disease: Phospholipid measurement
Phospholipid measurement
0.700 1.000 1 2011 2011
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: 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: 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: 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: rs174479
rs174479
11 61911282 intron variant C/G snv 0.17
CUI: C0202177
Disease: Phospholipid measurement
Phospholipid measurement
0.700 1.000 1 2011 2011
dbSNP: rs79972157
rs79972157
11 61934995 upstream gene variant C/G snv 3.8E-02
CUI: C0523829
Disease: Phosphatidylcholine measurement
Phosphatidylcholine measurement
0.700 1.000 1 2019 2019
dbSNP: rs17156580
rs17156580
11 61924869 upstream gene variant C/T snv 5.6E-02
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
0.700 1.000 1 2012 2012
dbSNP: rs174469
rs174469
11 61899971 intron variant C/T snv 0.14
CUI: C0202177
Disease: Phospholipid measurement
Phospholipid measurement
0.700 1.000 1 2011 2011
dbSNP: rs174471
rs174471
11 61902565 intron variant C/T snv 0.32 0.29
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: 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: rs76368648
rs76368648
11 61943400 intergenic variant C/T snv 4.1E-02
CUI: C0523829
Disease: Phosphatidylcholine measurement
Phosphatidylcholine measurement
0.700 1.000 1 2019 2019