RS139644798 RARS1

Health Risk Chr 5:168510601
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What This Variant Does
"RARS gene, c.1367C&gt
Associated Conditions
Hypomyelinating leukodystrophy 9
Inborn genetic diseases
Hypomyelinating leukodystrophy 9
Inborn genetic diseases
Other Variants in RARS1
rs672601372 rs672601373 rs672601374 rs672601375 rs369398935 rs1064792894 rs1057518618 rs769713780 rs768923402 rs754997301
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