RS1064794841 NFIA

Health Risk Chr 1:61088191
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What This Variant Does
"CLNSIG=4
Associated Conditions
Chromosome 1p32-p31 deletion syndrome
Brain malformations with or without urinary tract defects
Chromosome 1p32-p31 deletion syndrome
Brain malformations with or without urinary tract defects
Other Variants in NFIA
rs886039429 rs1057518992 rs1060505054 rs1064796492 rs1553149202 rs1553180342 rs1553149185 rs1553167851 rs1553149167 rs1553149206
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