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: rs10207392
rs10207392
ACOXL ; MIR4435-2HG
2 2 111092082 intron variant A/G snv 0.48 0.700 1.000 1 2012 2012
dbSNP: rs143800403
rs143800403
MIR4435-2HG
1 2 111373568 intron variant C/A;T snv 0.700 1.000 1 2016 2016
dbSNP: rs1448203
rs1448203
MIR4435-2HG ; SOCAR
1 2 111510708 non coding transcript exon variant T/A;C snv 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: rs62160676
rs62160676
MIR4435-2HG
5 2 111410354 intron variant T/C;G snv 0.700 1.000 1 2016 2016