Source: GWASCAT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs2517532
rs2517532 		0.925 0.120 6 31050630 upstream gene variant A/G snv 0.60
CUI: C0020676
Disease: Hypothyroidism
Hypothyroidism 		0.800 1.000 1 2012 2012
dbSNP: rs3129720
rs3129720 		0.851 0.280 6 32695854 intergenic variant T/C snv 0.76
CUI: C0020676
Disease: Hypothyroidism
Hypothyroidism 		0.800 1.000 1 2012 2012
dbSNP: rs4915077
rs4915077
VAV3
1.000 0.040 1 107823394 intron variant T/C snv 9.0E-02
CUI: C0020676
Disease: Hypothyroidism
Hypothyroidism 		0.800 1.000 1 2012 2012
dbSNP: rs6679677
rs6679677
PHTF1
0.653 0.320 1 113761186 upstream gene variant C/A snv 6.7E-02
CUI: C0020676
Disease: Hypothyroidism
Hypothyroidism 		0.800 1.000 1 2012 2012
dbSNP: rs925489
rs925489
PTCSC2
0.882 0.080 9 97784318 intron variant C/T snv 0.71
CUI: C0020676
Disease: Hypothyroidism
Hypothyroidism 		0.800 1.000 1 2011 2012
dbSNP: rs948426
rs948426
LINC01387 ; LOC105371972
1.000 0.040 18 6567183 intron variant A/G snv 0.30
CUI: C0020676
Disease: Hypothyroidism
Hypothyroidism 		0.800 1.000 1 2012 2012
dbSNP: rs10223666
rs10223666
LOC105375069 ; LOC107986598
1.000 0.040 6 43837765 intron variant G/A;C snv
CUI: C0020676
Disease: Hypothyroidism
Hypothyroidism 		0.700 1.000 1 2016 2016
dbSNP: rs10759927
rs10759927
PTCSC2
1.000 0.040 9 97779894 intron variant A/G snv 0.72
CUI: C0020676
Disease: Hypothyroidism
Hypothyroidism 		0.700 1.000 1 2016 2016
dbSNP: rs10774625
rs10774625
ATXN2
0.763 0.320 12 111472415 intron variant A/G snv 0.66
CUI: C0020676
Disease: Hypothyroidism
Hypothyroidism 		0.700 1.000 1 2016 2016
dbSNP: rs10821973
rs10821973
LINC02621
1.000 0.040 10 62292578 intron variant G/A;C snv
CUI: C0020676
Disease: Hypothyroidism
Hypothyroidism 		0.700 1.000 1 2016 2016
dbSNP: rs12138950
rs12138950
MICOS10 ; LOC105376817 ; LOC105376818 ; LOC105376819
0.925 0.040 1 19512621 intron variant A/C snv 5.4E-03
CUI: C0020676
Disease: Hypothyroidism
Hypothyroidism 		0.700 1.000 1 2016 2016
dbSNP: rs121912648
rs121912648
TG
0.925 0.040 8 132882609 stop gained C/T snv 3.6E-04 4.0E-04
CUI: C0020676
Disease: Hypothyroidism
Hypothyroidism 		0.700 1.000 1 2016 2016
dbSNP: rs1479567
rs1479567
PDE8B
1.000 0.040 5 77232197 intron variant G/A;C snv
CUI: C0020676
Disease: Hypothyroidism
Hypothyroidism 		0.700 1.000 1 2016 2016
dbSNP: rs17020055
rs17020055
VAV3
1.000 0.040 1 107793911 intron variant A/C snv 0.11
CUI: C0020676
Disease: Hypothyroidism
Hypothyroidism 		0.800 1.000 1 2012 2016
dbSNP: rs1861628
rs1861628
LOC101928278
1.000 0.040 2 216763707 intron variant A/G snv 0.65
CUI: C0020676
Disease: Hypothyroidism
Hypothyroidism 		0.700 1.000 1 2016 2016
dbSNP: rs201295667
rs201295667 		1.000 0.040 20 22649878 intergenic variant C/- del 8.5E-04
CUI: C0020676
Disease: Hypothyroidism
Hypothyroidism 		0.700 1.000 1 2016 2016
dbSNP: rs2466075
rs2466075
NRG1
1.000 0.040 8 32575431 intron variant A/G snv 0.51
CUI: C0020676
Disease: Hypothyroidism
Hypothyroidism 		0.700 1.000 1 2016 2016
dbSNP: rs661713
rs661713
BACH2
1.000 0.040 6 90266280 intron variant G/A snv 0.69
CUI: C0020676
Disease: Hypothyroidism
Hypothyroidism 		0.700 1.000 1 2016 2016
dbSNP: rs6914622
rs6914622
SASH1
0.851 0.040 6 148193165 regulatory region variant G/T snv 0.33
CUI: C0020676
Disease: Hypothyroidism
Hypothyroidism 		0.700 1.000 1 2016 2016
dbSNP: rs7193703
rs7193703
CDH13
1.000 0.040 16 83624538 intron variant A/G snv 9.9E-03
CUI: C0020676
Disease: Hypothyroidism
Hypothyroidism 		0.700 1.000 1 2016 2016
dbSNP: rs7312770
rs7312770 		0.925 0.120 12 56073803 upstream gene variant C/T snv 0.53
CUI: C0020676
Disease: Hypothyroidism
Hypothyroidism 		0.700 1.000 1 2016 2016
dbSNP: rs7508679
rs7508679
INSR
1.000 0.040 19 7222821 intron variant T/C snv 0.61
CUI: C0020676
Disease: Hypothyroidism
Hypothyroidism 		0.700 1.000 1 2016 2016
dbSNP: rs76342258
rs76342258
LOC107986195
1.000 0.040 4 148710641 intron variant G/T snv 0.13
CUI: C0020676
Disease: Hypothyroidism
Hypothyroidism 		0.700 1.000 1 2016 2016
dbSNP: rs9273370
rs9273370
HLA-DQB1-AS1
1.000 0.040 6 32658715 upstream gene variant G/A snv 0.57
CUI: C0020676
Disease: Hypothyroidism
Hypothyroidism 		0.700 1.000 1 2016 2016
dbSNP: rs9511143
rs9511143
SPATA13
1.000 0.040 13 24200509 intron variant C/T snv 0.56
CUI: C0020676
Disease: Hypothyroidism
Hypothyroidism 		0.700 1.000 1 2016 2016