Disease: Triiodothyronine measurement
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs12534332
LOC105375586
7 155214802 intron variant G/A snv 0.59 2
rs2066773
MAPK12
22 50257071 non coding transcript exon variant G/A;C snv 2.0E-02; 4.0E-06 2
rs67142165
EPHB2
1 22884066 intron variant C/T snv 8.2E-02 2
rs7020640
HSPC324 ; LOC102724193 ; EGFL7
9 136653172 intron variant C/T snv 0.21 2
rs749618 19 52112198 upstream gene variant A/G snv 0.13 2
rs76465767 12 122901948 TF binding site variant T/C snv 2.4E-02 2