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: rs10220668
rs10220668
LINC01500
1.000 0.040 14 59042487 intron variant A/G snv 0.30
CUI: C0036421
Disease: Systemic Scleroderma
Systemic Scleroderma 		0.700 1.000 1 2013 2013
dbSNP: rs1432096
rs1432096
LINC01500
1.000 0.080 14 58718338 intron variant G/A;T snv
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma 		0.700 1.000 1 2013 2013
dbSNP: rs17094971
rs17094971
LINC01500
1.000 0.080 14 58716480 intron variant A/T snv 0.13
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma 		0.700 1.000 1 2013 2013
dbSNP: rs17833380
rs17833380
LINC01500
1.000 0.080 14 58917038 intron variant C/T snv 0.15
CUI: C0027404
Disease: Narcolepsy
Narcolepsy 		0.700 1.000 1 2009 2009
dbSNP: rs311844
rs311844
LINC01500
1.000 0.080 14 58672253 intron variant G/T snv 0.19
CUI: C0027404
Disease: Narcolepsy
Narcolepsy 		0.700 1.000 1 2009 2009
dbSNP: rs405460
rs405460
LINC01500
14 58899597 intron variant G/A;T snv
CUI: C0162701
Disease: Polysomnography
Polysomnography 		0.700 1.000 1 2012 2012
dbSNP: rs7141538
rs7141538
LINC01500
1.000 0.080 14 58717811 intron variant C/T snv 0.17
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma 		0.700 1.000 1 2013 2013