Gene: LINC01748 ×
Source: ALL
Variant Gene N. diseases v DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs472913
rs472913
LINC01748
1 1.000 0.040 1 60629886 intron variant G/C;T snv 0.800 1.000 1 2009 2009
dbSNP: rs10889182
rs10889182
LINC01748
1 1.000 0.040 1 60532523 intron variant T/G snv 0.33 0.700 1.000 1 2013 2013
dbSNP: rs10889187
rs10889187
LINC01748
1 1.000 0.040 1 60545086 intron variant G/A snv 0.33 0.700 1.000 1 2013 2013
dbSNP: rs10889189
rs10889189
LINC01748
1 1.000 0.040 1 60559354 intron variant C/G snv 0.47 0.700 1.000 1 2013 2013
dbSNP: rs11207633
rs11207633
LINC01748
1 1.000 0.040 1 60541510 non coding transcript exon variant A/G snv 0.32 0.700 1.000 1 2013 2013