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: rs1779410
rs1779410
TMCC2
1 1 205279631 intron variant A/C;G snv 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: rs61823972
rs61823972
TMCC2
4 1 205232197 intron variant A/C;T snv 0.700 1.000 1 2016 2016
dbSNP: rs1078362
rs1078362
TMCC2 ; LOC101929459
1 1 205240402 intron variant A/G snv 0.47 0.700 1.000 1 2012 2012
dbSNP: rs1172132
rs1172132
TMCC2
1 1 205273773 intron variant A/G snv 0.67 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: rs1768586
rs1768586
TMCC2
1 1 205269147 synonymous variant A/G snv 0.27 0.27 0.700 1.000 1 2012 2012
dbSNP: rs9660992
rs9660992
TMCC2
2 1 205280322 intron variant A/G snv 0.43 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: rs4400674
rs4400674
TMCC2
1 1 205249297 intron variant C/A snv 0.27 0.700 1.000 1 2012 2012
dbSNP: rs1768585
rs1768585
TMCC2
1 1 205269993 intron variant C/A;G;T snv 0.700 1.000 1 2012 2012
dbSNP: rs1779411
rs1779411
TMCC2
1 1 205269402 synonymous variant C/G;T snv 0.26 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: rs1151785
rs1151785
TMCC2
1 1 205263171 intron variant C/T snv 0.25 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: rs1177720
rs1177720
TMCC2
1 1 205265300 intron variant C/T snv 0.67 0.700 1.000 1 2012 2012
dbSNP: rs1668867
rs1668867
TMCC2
1 1 205271123 synonymous variant C/T snv 0.27 0.28 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: rs1151787
rs1151787
TMCC2
1 1 205285110 intron variant G/A 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: rs1172130
rs1172130
TMCC2
2 1 205275825 intron variant G/A snv 0.30 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: rs1172140
rs1172140
TMCC2
1 1 205243896 intron variant G/A snv 0.49 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: rs1668873
rs1668873
TMCC2
2 1 205266862 intron variant G/A snv 0.27 0.700 1.000 1 2012 2012