RS372966991 GLA;HNRNPH2;RPL36A-HNRNPH2

Health Risk Chr X:101403845
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What This Variant Does
"CLNSIG=5
Associated Conditions
Fabry disease
Cardiovascular phenotype
Fabry disease
Cardiovascular phenotype
Fabry disease
Cardiovascular phenotype
Fabry disease
Cardiovascular phenotype
Other Variants in GLA;HNRNPH2;RPL36A-HNRNPH2
rs782312723
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