Gene: LINC01876 ×
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: rs17244395
rs17244395
LINC01876
1 2 156060013 intron variant T/C snv 7.9E-02 0.700 1.000 1 2018 2018
dbSNP: rs17244416
rs17244416
LINC01876
1 2 156060314 intron variant G/C snv 7.9E-02 0.700 1.000 1 2018 2018
dbSNP: rs72904190
rs72904190
LINC01876
1 2 156027428 intron variant A/G snv 7.4E-02 0.700 1.000 1 2019 2019
dbSNP: rs72906060
rs72906060
LINC01876
2 1.000 0.040 2 156053895 intron variant T/C snv 8.4E-02 0.700 1.000 1 2019 2019
dbSNP: rs72906064
rs72906064
LINC01876
1 2 156055088 intron variant G/T snv 7.9E-02 0.700 1.000 1 2019 2019