CLTCL1, clathrin heavy chain like 1, 8218

N. diseases: 9; N. variants: 62
Disease: Serum albumin measurement ×
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: rs2073754
rs2073754 		22 19233883 intron variant T/G snv 0.38
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2012 2012
dbSNP: rs1018764
rs1018764 		22 19184493 3 prime UTR variant T/C snv 0.75 0.75
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2012 2012
dbSNP: rs1061325
rs1061325 		22 19196584 missense variant T/C snv 0.49 0.43
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2012 2012
dbSNP: rs1780643
rs1780643 		22 19204215 intron variant T/C snv 0.75
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2012 2012
dbSNP: rs2854643
rs2854643 		22 19202196 intron variant T/C snv 0.75
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2012 2012
dbSNP: rs361991
rs361991 		22 19276369 intron variant T/C snv 0.39
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2012 2012
dbSNP: rs362148
rs362148 		22 19275329 intron variant T/C snv 0.39
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2012 2012
dbSNP: rs712958
rs712958 		22 19179896 3 prime UTR variant T/C snv 0.69
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2012 2012
dbSNP: rs756651
rs756651 		22 19191855 intron variant T/C snv 0.75
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2012 2012
dbSNP: rs885979
rs885979 		22 19210865 intron variant T/C snv 0.68
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2012 2012
dbSNP: rs9605972
rs9605972 		22 19265751 intron variant T/C snv 0.38
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2012 2012
dbSNP: rs1780639
rs1780639 		22 19187091 intron variant T/A;C snv
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2012 2012
dbSNP: rs1780642
rs1780642 		22 19183091 non coding transcript exon variant T/A;C snv
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2012 2012
dbSNP: rs2800973
rs2800973 		22 19181103 non coding transcript exon variant T/A;C snv 0.76
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2012 2012
dbSNP: rs698423
rs698423 		22 19210386 synonymous variant T/A;C snv 4.0E-06; 0.74
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2012 2012
dbSNP: rs1771540
rs1771540 		22 19186421 intron variant T/A snv 0.75
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2012 2012
dbSNP: rs4819508
rs4819508 		22 19269947 intron variant T/A snv 0.59
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2012 2012
dbSNP: rs9605960
rs9605960 		22 19227113 intron variant G/C snv 0.38
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2012 2012
dbSNP: rs807458
rs807458 		22 19233125 intron variant G/A;T snv 6.5E-02; 0.42
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2012 2012
dbSNP: rs2800974
rs2800974 		22 19180574 intron variant G/A;C snv
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2012 2012
dbSNP: rs5748028
rs5748028 		22 19184768 non coding transcript exon variant G/A snv 0.68
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2012 2012
dbSNP: rs723414
rs723414 		22 19198225 intron variant G/A snv 0.65
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2012 2012
dbSNP: rs807431
rs807431 		22 19254838 intron variant G/A snv 0.62
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2012 2012
dbSNP: rs9605957
rs9605957 		22 19199864 non coding transcript exon variant G/A snv 0.57 0.54
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2012 2012
dbSNP: rs1206544
rs1206544 		22 19227516 intron variant C/T snv 0.62
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2012 2012