Gene: RMI2 ×
Source: GWASDB ×
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: rs1646019
rs1646019
RMI2 ; LOC105371082
1 1.000 0.080 16 11265823 intron variant C/T snv 0.36 0.800 1.000 1 2012 2012
dbSNP: rs243325
rs243325
RMI2 ; LOC105371082
1 1.000 0.080 16 11260640 intron variant T/C snv 0.38 0.710 1.000 2 2012 2012
dbSNP: rs243323
rs243323
RMI2 ; LOC105371082
1 1.000 0.080 16 11267345 intron variant A/C;G;T snv 0.700 1.000 2 2012 2012
dbSNP: rs188754154
rs188754154
SOCS1 ; RMI2 ; LOC105371082
1 1.000 0.080 16 11255517 5 prime UTR variant T/A snv 3.8E-03 4.1E-03 0.700 1.000 1 2012 2012
dbSNP: rs243317
rs243317
RMI2 ; LOC105371082
1 1.000 0.080 16 11263474 intron variant A/C;T snv 0.700 1.000 1 2012 2012
dbSNP: rs243318
rs243318
RMI2 ; LOC105371082
1 1.000 0.080 16 11264161 intron variant G/A snv 0.38 0.700 1.000 1 2012 2012
dbSNP: rs413024
rs413024
RMI2 ; LOC105371082
1 1.000 0.080 16 11260234 intron variant A/G snv 0.26 0.700 1.000 1 2012 2012
dbSNP: rs4780355
rs4780355
SOCS1 ; RMI2 ; LOC105371082
2 0.882 0.120 16 11254001 intron variant T/C;G snv 0.700 1.000 1 2012 2012