Gene: SLC6A13 ×
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: rs10774020
rs10774020
SLC6A13
1 12 239710 intron variant T/C snv 0.58 0.700 1.000 2 2019 2019
dbSNP: rs11062167
rs11062167
SLC6A13 ; LOC102723544
2 12 255573 intron variant G/A snv 0.36 0.700 1.000 2 2017 2019
dbSNP: rs10774021
rs10774021
SLC6A13
4 1.000 0.080 12 240132 intron variant C/T snv 0.57 0.700 1.000 1 2016 2016
dbSNP: rs11062070
rs11062070
SLC6A13
1 12 234466 intron variant C/T snv 0.69 0.700 1.000 1 2018 2018
dbSNP: rs11062102
rs11062102
SLC6A13
1 12 239619 intron variant T/C snv 0.58 0.700 1.000 1 2019 2019
dbSNP: rs7969761
rs7969761
SLC6A13
1 12 246676 intron variant C/T snv 0.44 0.700 1.000 1 2019 2019