Source: GWASDB

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: rs7024345
rs7024345
PTCSC2
0.925 0.080 9 97832956 intron variant A/G snv 0.82
CUI: C0020676
Disease: Hypothyroidism
Hypothyroidism 		0.700 1.000 1 2012 2012
dbSNP: rs7024345
rs7024345
PTCSC2
0.925 0.080 9 97832956 intron variant A/G snv 0.82
CUI: C0549473
Disease: Thyroid carcinoma
Thyroid carcinoma 		0.700 1.000 1 2009 2009