RS774923951 RARS2

Health Risk Chr 6:87589957
Upload your DNA to see your genotype for this variant.
What This Variant Does
"CLNSIG=5
Associated Conditions
Inborn genetic diseases
Pontocerebellar hypoplasia type 6
Pontocerebellar hypoplasia type 6
Pontocerebellar hypoplasia type 6
Inborn genetic diseases
Pontocerebellar hypoplasia type 6
Pontocerebellar hypoplasia type 6
Pontocerebellar hypoplasia type 6
Other Variants in RARS2
rs63749985 rs387907048 rs147391618 rs141374913 rs145189950 rs199941996 rs138360045 rs756696262 rs756502974 rs142348911
Ask Dr. Hemsworth about this variant