Gene: SLC22A2 ×
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: rs2279463
rs2279463
SLC22A2
4 1.000 0.080 6 160247357 intron variant A/G;T snv 0.700 1.000 5 2016 2019
dbSNP: rs316009
rs316009
SLC22A2
2 6 160254732 intron variant T/C;G snv 0.700 1.000 2 2016 2016
dbSNP: rs316020
rs316020
SLC22A2
2 6 160248049 intron variant A/G snv 0.89 0.700 1.000 2 2018 2019
dbSNP: rs12207180
rs12207180
SLC22A2
2 1.000 0.080 6 160212075 intron variant T/A;G snv 0.12 0.700 1.000 1 2019 2019
dbSNP: rs145590578
rs145590578
SLC22A2
3 1.000 0.040 6 160236104 intron variant GTT/- delins 9.8E-02 0.700 1.000 1 2019 2019
dbSNP: rs3101823
rs3101823
SLC22A2
1 6 160240136 intron variant T/G snv 9.8E-02 0.700 1.000 1 2019 2019
dbSNP: rs515140
rs515140
SLC22A2
1 6 160227235 intron variant T/G snv 0.72 0.700 1.000 1 2019 2019