Source: CURATED

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: rs13361707
rs13361707
0.882 0.120 5 40791782 intron variant C/T snv 0.31
CUI: C0699791
Disease: Stomach Carcinoma
Stomach Carcinoma
0.780 1.000 3 2011 2018
dbSNP: rs13361707
rs13361707
0.882 0.120 5 40791782 intron variant C/T snv 0.31
CUI: C0024623
Disease: Malignant neoplasm of stomach
Malignant neoplasm of stomach
0.780 1.000 1 2011 2018
dbSNP: rs13361707
rs13361707
0.882 0.120 5 40791782 intron variant C/T snv 0.31
CUI: C0036341
Disease: Schizophrenia
Schizophrenia
0.700 1.000 1 2011 2011