Gene: LINC01894 ×
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: rs10502463
rs10502463
LINC01894
1 1.000 0.040 18 24981789 intron variant G/A snv 0.29 0.700 1.000 1 2017 2017
dbSNP: rs16941126
rs16941126
LINC01894
1 1.000 0.040 18 24976475 intron variant A/G snv 8.1E-02 0.700 1.000 1 2017 2017
dbSNP: rs17188256
rs17188256
LINC01894
1 1.000 0.040 18 24975135 intron variant T/G snv 4.1E-02 0.700 1.000 1 2017 2017
dbSNP: rs17204304
rs17204304
LINC01894
1 1.000 0.040 18 24984047 intron variant C/A;T snv 0.700 1.000 1 2017 2017
dbSNP: rs17798760
rs17798760
LINC01894
1 1.000 0.040 18 24979684 intron variant A/T snv 0.10 0.700 1.000 1 2017 2017
dbSNP: rs17798772
rs17798772
LINC01894
1 1.000 0.040 18 24981700 intron variant A/G snv 6.6E-02 0.700 1.000 1 2017 2017
dbSNP: rs2187004
rs2187004
LINC01894
1 1.000 0.040 18 24978357 intron variant C/A;T snv 0.700 1.000 1 2017 2017
dbSNP: rs4496242
rs4496242
LINC01894
1 1.000 0.040 18 24980444 intron variant A/G snv 0.32 0.700 1.000 1 2017 2017