Gene: MIR4435-2HG ×
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: rs62160676
rs62160676
MIR4435-2HG
5 2 111410354 intron variant T/C;G snv 0.700 1.000 2 2016 2019
dbSNP: rs112744032
rs112744032
MIR4435-2HG ; SOCAR
1 2 111521757 intron variant G/- delins 0.700 1.000 1 2016 2016
dbSNP: rs143326447
rs143326447
MIR4435-2HG ; SOCAR
4 0.925 0.080 2 111511155 intron variant T/C snv 0.11 0.700 1.000 1 2019 2019
dbSNP: rs2009581
rs2009581
ACOXL ; MIR4435-2HG
3 2 111050100 intron variant G/A snv 0.26 0.700 1.000 1 2019 2019
dbSNP: rs2139376
rs2139376
MIR4435-2HG
2 2 111385836 intron variant T/C snv 0.44 0.700 1.000 1 2019 2019
dbSNP: rs2334232
rs2334232
MIR4435-2HG
1 2 111371516 intron variant G/A snv 0.18 0.700 1.000 1 2016 2016
dbSNP: rs4848370
rs4848370
ACOXL ; MIR4435-2HG
2 2 111054088 intron variant C/T snv 0.25 0.700 1.000 1 2016 2016
dbSNP: rs604126
rs604126
MIR4435-2HG
1 2 111185623 intron variant A/C;G;T snv 0.700 1.000 1 2019 2019
dbSNP: rs616582
rs616582
MIR4435-2HG
1 2 111184418 intron variant T/C;G snv 0.700 1.000 1 2016 2016