RS769713780 RARS1

Health Risk Chr 5:168486500
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What This Variant Does
"CLNSIG=5
Associated Conditions
Hypomyelinating leukodystrophy 9
Inborn genetic diseases
Hypomyelinating leukodystrophy 9
Inborn genetic diseases
Other Variants in RARS1
rs672601372 rs672601373 rs672601374 rs672601375 rs369398935 rs139644798 rs1064792894 rs1057518618 rs768923402 rs754997301
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