Gene: TMCC2 ×
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: rs61823972
rs61823972
TMCC2
4 1 205232197 intron variant A/C;T snv 0.700 1.000 1 2016 2016
dbSNP: rs896320
rs896320
TMCC2 ; LOC101929459
1 1 205236219 intron variant T/A;C snv 0.700 1.000 1 2012 2012
dbSNP: rs1172161
rs1172161
TMCC2 ; LOC101929459
1 1 205237367 intron variant C/T snv 0.27 0.700 1.000 1 2012 2012
dbSNP: rs1172159
rs1172159
TMCC2 ; LOC101929459
1 1 205238384 intron variant T/C snv 0.27 0.700 1.000 1 2012 2012
dbSNP: rs1078362
rs1078362
TMCC2 ; LOC101929459
1 1 205240402 intron variant A/G snv 0.47 0.700 1.000 1 2012 2012
dbSNP: rs1172140
rs1172140
TMCC2
1 1 205243896 intron variant G/A snv 0.49 0.700 1.000 1 2012 2012
dbSNP: rs1172139
rs1172139
TMCC2
1 1 205244834 intron variant G/A snv 0.27 0.700 1.000 1 2012 2012
dbSNP: rs748012
rs748012
TMCC2
2 1 205247445 intron variant G/A snv 0.27 0.700 1.000 1 2012 2012
dbSNP: rs4400674
rs4400674
TMCC2
1 1 205249297 intron variant C/A snv 0.27 0.700 1.000 1 2012 2012
dbSNP: rs1172156
rs1172156
TMCC2
1 1 205250959 intron variant G/A snv 0.49 0.700 1.000 1 2012 2012
dbSNP: rs1172154
rs1172154
TMCC2
1 1 205251511 intron variant T/G snv 0.49 0.700 1.000 1 2012 2012
dbSNP: rs1172153
rs1172153
TMCC2
1 1 205251533 intron variant T/C snv 0.49 0.700 1.000 1 2012 2012
dbSNP: rs1172152
rs1172152
TMCC2
1 1 205251590 intron variant T/A snv 0.29 0.700 1.000 1 2012 2012
dbSNP: rs1172151
rs1172151
TMCC2
1 1 205252531 intron variant T/G snv 0.49 0.700 1.000 1 2012 2012
dbSNP: rs1172150
rs1172150
TMCC2
1 1 205252733 intron variant A/G;T snv 0.700 1.000 1 2012 2012
dbSNP: rs1172149
rs1172149
TMCC2
2 1 205255630 intron variant A/G snv 0.51 0.700 1.000 1 2012 2012
dbSNP: rs1172147
rs1172147
TMCC2
1 1 205256329 splice acceptor variant G/A;T snv 0.28 0.700 1.000 1 2012 2012
dbSNP: rs1151785
rs1151785
TMCC2
1 1 205263171 intron variant C/T snv 0.25 0.700 1.000 1 2012 2012
dbSNP: rs1151784
rs1151784
TMCC2
1 1 205263319 intron variant C/T snv 0.25 0.700 1.000 1 2012 2012
dbSNP: rs1172111
rs1172111
TMCC2
1 1 205263852 intron variant G/A snv 0.27 0.700 1.000 1 2012 2012
dbSNP: rs1177720
rs1177720
TMCC2
1 1 205265300 intron variant C/T snv 0.67 0.700 1.000 1 2012 2012
dbSNP: rs7367930
rs7367930
TMCC2
1 1 205266384 intron variant A/C;G snv 0.700 1.000 1 2012 2012
dbSNP: rs1668873
rs1668873
TMCC2
2 1 205266862 intron variant G/A snv 0.27 0.700 1.000 1 2012 2012
dbSNP: rs1768587
rs1768587
TMCC2
1 1 205267304 intron variant C/T snv 0.25 0.700 1.000 1 2012 2012
dbSNP: rs1668871
rs1668871
TMCC2
2 1 205268009 intron variant T/C;G snv 0.700 1.000 1 2012 2012