rs1443438, PTCSC2

N. diseases: 8
Source: ALL
Disease N. SNPs d DSI v DPI v Chr Position Consequence Alleles Class AFEXOME AFGENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
AUTOIMMUNE DISEASE, MULTISYSTEM, INFANTILE-ONSET, 1
142 0.827 0.080 9 97787746 intron variant T/A;C snv 0.700 1.000 1 2019 2019
AUTOIMMUNE DISEASE, MULTISYSTEM, INFANTILE-ONSET, 2
132 0.827 0.080 9 97787746 intron variant T/A;C snv 0.700 1.000 1 2019 2019
AUTOIMMUNE DISEASE, SUSCEPTIBILITY TO, 6
141 0.827 0.080 9 97787746 intron variant T/A;C snv 0.700 1.000 1 2019 2019
Autoimmune Diseases
CUI: C0004364
Disease: Autoimmune Diseases
428 0.827 0.080 9 97787746 intron variant T/A;C snv 0.700 1.000 1 2019 2019
Hypothyroidism
CUI: C0020676
Disease: Hypothyroidism
283 0.827 0.080 9 97787746 intron variant T/A;C snv 0.700 1.000 1 2012 2012
Polysomnography
CUI: C0162701
Disease: Polysomnography
249 0.827 0.080 9 97787746 intron variant T/A;C snv 0.700 1.000 1 2012 2012
Thyroid carcinoma
CUI: C0549473
Disease: Thyroid carcinoma
145 0.827 0.080 9 97787746 intron variant T/A;C snv 0.700 1.000 1 2013 2013
Thyroid stimulating hormone measurement
83 0.827 0.080 9 97787746 intron variant T/A;C snv 0.700 1.000 1 2012 2012