RS869312967 SLC27A4

Health Risk Chr 9:128355796
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What This Variant Does
"CLNSIG=5
Associated Conditions
Inborn genetic diseases
Inborn genetic diseases
Other Variants in SLC27A4
rs137853131 rs1588559786 rs137853132 rs137853134 rs764922350 rs587776384 rs368207076 rs140481562 rs765311079 rs758657421
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