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: rs1668869
rs1668869
TMCC2
1 1 205270651 intron variant G/C 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
dbSNP: rs1668873
rs1668873
TMCC2
2 1 205266862 intron variant G/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: rs1768586
rs1768586
TMCC2
1 1 205269147 synonymous variant A/G snv 0.27 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: rs1779410
rs1779410
TMCC2
1 1 205279631 intron variant A/C;G 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: rs4400674
rs4400674
TMCC2
1 1 205249297 intron variant C/A snv 0.27 0.700 1.000 1 2012 2012
dbSNP: rs4951184
rs4951184
TMCC2
1 1 205271531 intron variant T/A snv 0.27 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: rs7367930
rs7367930
TMCC2
1 1 205266384 intron variant A/C;G snv 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: rs896320
rs896320
TMCC2 ; LOC101929459
1 1 205236219 intron variant T/A;C snv 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