Gene: MTCH2 ×
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: rs3817334
rs3817334
MTCH2
7 1.000 0.080 11 47629441 intron variant C/T snv 0.36 0.700 1.000 8 2010 2018
dbSNP: rs1064608
rs1064608
MTCH2
1 11 47618877 missense variant G/C;T snv 0.32; 8.0E-06 0.700 1.000 1 2018 2018
dbSNP: rs10838738
rs10838738
MTCH2
6 1.000 0.080 11 47641497 intron variant A/G snv 0.28 0.700 1.000 1 2009 2009