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: rs1151786
rs1151786
TMCC2
1 1 205258632 intron variant G/A;C;T snv 0.700 1.000 1 2016 2016
dbSNP: rs61823972
rs61823972
TMCC2
4 1 205232197 intron variant A/C;T snv 0.700 1.000 1 2016 2016