SLC17A3, solute carrier family 17 member 3, 10786

N. diseases: 21; N. variants: 64
Disease: Red Blood Cell Count measurement ×
Source: ALL
Variant DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Disease Class Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs17271121
rs17271121 		0.925 0.120 6 25863422 intron variant T/C snv 8.9E-02
CUI: C0014772
Disease: Red Blood Cell Count measurement
Red Blood Cell Count measurement 		0.700 1.000 1 2009 2009
dbSNP: rs3887266
rs3887266 		0.925 0.120 6 25843518 intron variant C/T snv 8.9E-02
CUI: C0014772
Disease: Red Blood Cell Count measurement
Red Blood Cell Count measurement 		0.700 1.000 1 2009 2009
dbSNP: rs717551
rs717551 		6 25855396 intron variant T/C snv 0.16
CUI: C0014772
Disease: Red Blood Cell Count measurement
Red Blood Cell Count measurement 		0.700 1.000 1 2009 2009