Gene: SLC47A1 ×
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: rs2252281
rs2252281
SLC47A1
2 1.000 0.120 17 19533874 5 prime UTR variant T/C snv 0.32 0.700 1.000 2 2019 2019
dbSNP: rs11871125
rs11871125
SLC47A1
1 17 19529080 intron variant C/A;G;T snv 0.700 1.000 1 2019 2019
dbSNP: rs2440164
rs2440164
SLC47A1
1 17 19525297 intron variant A/G snv 0.33 0.700 1.000 1 2019 2019
dbSNP: rs2440165
rs2440165
SLC47A1
2 1.000 0.080 17 19525406 intron variant T/C snv 0.33 0.700 1.000 1 2019 2019
dbSNP: rs2453580
rs2453580
SLC47A1
4 17 19535008 non coding transcript exon variant T/C snv 0.37 0.700 1.000 1 2016 2016
dbSNP: rs2453583
rs2453583
SLC47A1
1 17 19538723 intron variant A/T snv 0.33 0.700 1.000 1 2019 2019
dbSNP: rs2453584
rs2453584
SLC47A1
1 17 19540132 intron variant G/C snv 0.29 0.700 1.000 1 2019 2019
dbSNP: rs894680
rs894680
SLC47A1
2 17 19537225 intron variant G/A snv 0.29 0.700 1.000 1 2017 2017