Gene: LINC01376 ×
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: rs12710696
rs12710696
LINC01376
2 0.925 0.080 2 19121042 intron variant T/A;C snv 0.710 1.000 4 2013 2017
dbSNP: rs10169133
rs10169133
LINC01376
1 1.000 0.080 2 19212878 intron variant G/C;T snv 0.55 0.700 1.000 1 2017 2017
dbSNP: rs11684853
rs11684853
LINC01376
1 1.000 0.080 2 19111157 intron variant G/T snv 0.51 0.700 1.000 1 2017 2017