RS137853863 NSDHL

Health Risk Chr X:152869039 snv missense variant
Upload your DNA to see your genotype for this variant.
What This Variant Does
"[OMIM:?]
Associated Conditions
Child syndrome
Child syndrome
Population Frequencies
gnomAD ALL
100%
Other Variants in NSDHL
rs104894909 rs104894901 rs104894902 rs104894903 rs104894904 rs104894905 rs121909834 rs121909833 rs375100066 rs587784223
Ask Dr. Hemsworth about this variant