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: rs12420625
rs12420625 		11 61922933 upstream gene variant T/G snv 6.2E-02
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: 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: rs13966
rs13966 		11 61897520 3 prime UTR variant T/C snv 0.53
CUI: C0202177
Disease: Phospholipid measurement
Phospholipid measurement 		0.700 1.000 1 2011 2011
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: 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: 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: 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
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: rs2521568
rs2521568 		11 61933461 upstream gene variant G/C snv 9.5E-02
CUI: C0202177
Disease: Phospholipid measurement
Phospholipid measurement 		0.700 1.000 1 2011 2011
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: rs17764935
rs17764935 		11 61897285 downstream gene variant G/A snv 4.9E-02
CUI: C0202177
Disease: Phospholipid measurement
Phospholipid measurement 		0.700 1.000 1 2011 2011
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: rs17764935
rs17764935 		11 61897285 downstream gene variant G/A snv 4.9E-02
CUI: C1261502
Disease: Finding of Mean Corpuscular Hemoglobin
Finding of Mean Corpuscular Hemoglobin 		0.700 1.000 1 2019 2019
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: 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: 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: 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: 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: 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