Gene: BHMT ×
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: rs492842
rs492842
BHMT ; DMGDH
1 5 79114164 intron variant C/T snv 0.59 0.010 1.000 1 2017 2017
dbSNP: rs542852
rs542852
BHMT ; DMGDH
1 5 79113573 intron variant T/C snv 0.63 0.010 1.000 1 2017 2017