Gene: LINC01934 ×
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: rs13011751
rs13011751
LINC01934
1 2 181121038 intron variant A/T snv 0.23 0.700 1.000 1 2018 2018
dbSNP: rs6433895
rs6433895
LINC01934
1 2 181147287 intron variant A/C snv 0.31 0.700 1.000 1 2016 2016
dbSNP: rs6760805
rs6760805
LINC01934
1 2 181293112 intron variant A/G snv 0.34 0.700 1.000 1 2016 2016