RS139721632 RARS2

Health Risk Chr 6:87529601 snv missense variant
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What This Variant Does
"CLNSIG=4
Associated Conditions
Pontocerebellar hypoplasia type 6
Inborn genetic diseases
Pontocerebellar hypoplasia type 6
Pontocerebellar hypoplasia type 6
Inborn genetic diseases
Pontocerebellar hypoplasia type 6
Population Frequencies
gnomAD ALL
0%
Other Variants in RARS2
rs63749985 rs387907048 rs147391618 rs141374913 rs145189950 rs199941996 rs138360045 rs756696262 rs756502974 rs142348911
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