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: rs10226620
rs10226620
MAFK ; TMEM184A
4 1.000 0.040 7 1541881 3 prime UTR variant T/C snv 0.69 0.010 1.000 1 2017 2017
dbSNP: rs211105
rs211105
TPH1
4 1.000 11 18033757 intron variant T/G snv 0.19 0.010 1.000 1 2018 2018
dbSNP: rs3735656
rs3735656
MAFK
5 1.000 0.040 7 1541285 3 prime UTR variant C/G;T snv 0.010 1.000 1 2017 2017