Disease: Creatinine clearance measurement
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10827209
NRP1
10 33198261 intron variant A/C snv 0.23 2
rs79666748 18 43280443 upstream gene variant A/C snv 7.0E-02 2
rs9341664 6 77375469 intergenic variant A/C snv 0.51 2
rs4802
SNORD14E ; HSPA8
11 123057914 synonymous variant A/C;G snv 4.1E-06; 0.32 2
rs7109445
CLMP
11 123094779 intron variant A/C;G snv 2
rs10892961
CLMP
11 123093392 intron variant A/C;G;T snv 2
rs10054178
C5orf17
5 24059742 intron variant A/G snv 7.5E-02 2
rs11218976
CLMP
11 123090950 intron variant A/G snv 0.41 2
rs11926663
IGSF11
3 119125638 intron variant A/G snv 1.8E-02 2
rs4936767 11 123047451 upstream gene variant A/G snv 0.34 2
rs7035473
OLFM1
9 135121519 downstream gene variant A/G snv 0.11 2
rs7121616
CLMP
11 123095918 intron variant A/G snv 0.41 2
rs73055009
C5orf17
5 24058406 intron variant A/G snv 7.5E-02 2
rs113051092
C5orf17
5 24060490 intron variant A/T snv 7.4E-02 2
rs638452 11 56495642 upstream gene variant A/T snv 0.58 2
rs4435343 18 43322011 intergenic variant C/A;T snv 2
rs4936770
HSPA8 ; SNORD14E
11 123058167 intron variant C/A;T snv 2
rs72609945 8 26048781 upstream gene variant C/A;T snv 0.13 2
rs73055087
C5orf17
5 24062454 intron variant C/A;T snv 2
rs16893073
C5orf17
5 24072508 intron variant C/G;T snv 2
rs10056373
C5orf17
5 24069684 intron variant C/T snv 7.4E-02 2
rs10119043 9 135122706 downstream gene variant C/T snv 0.11 2
rs116965780 18 43300829 intergenic variant C/T snv 7.0E-02 2
rs141827060
IGSF11
3 119132020 intron variant C/T snv 1.8E-02 2
rs17062791
DLGAP2
8 1203431 intron variant C/T snv 0.14 2