Gene: SNX13 ×
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: rs4142995
rs4142995
SNX13
2 7 17879635 3 prime UTR variant G/A;T snv 0.800 1.000 3 2013 2018
dbSNP: rs6461354
rs6461354
SNX13
2 7 17874977 intron variant C/T snv 0.51 0.700 1.000 2 2018 2019
dbSNP: rs17138358
rs17138358
SNX13
1 7 17880630 3 prime UTR variant G/C snv 0.45 0.700 1.000 1 2017 2017
dbSNP: rs1917368
rs1917368
SNX13
1 7 17872129 intron variant G/A;T snv 0.700 1.000 1 2018 2018