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: 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: 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: rs174475
rs174475 		11 61905173 intron variant G/C snv 0.36
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2012 2012
dbSNP: rs174478
rs174478 		11 61911104 intron variant T/G snv 0.31
CUI: C0202177
Disease: Phospholipid measurement
Phospholipid measurement 		0.700 1.000 1 2011 2011
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: 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: rs666870
rs666870 		11 61910007 intron variant G/A snv 0.30
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: 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: 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: 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: rs74556176
rs74556176 		11 61943075 intergenic variant G/A snv 4.1E-02
CUI: C0523829
Disease: Phosphatidylcholine measurement
Phosphatidylcholine measurement 		0.700 1.000 1 2019 2019
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
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: 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: rs2521572
rs2521572 		11 61944003 regulatory region variant T/G snv 0.91
CUI: C0202177
Disease: Phospholipid measurement
Phospholipid measurement 		0.700 1.000 1 2011 2011
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: rs2727261
rs2727261 		11 61944659 regulatory region variant T/C;G snv
CUI: C0202177
Disease: Phospholipid measurement
Phospholipid measurement 		0.700 1.000 1 2011 2011
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: rs174477
rs174477 		11 61908172 missense variant T/C snv 1.0E-01 0.11
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