RS587784223 NSDHL

Health Risk Chr X:152865870
Upload your DNA to see your genotype for this variant.
What This Variant Does
"CLNSIG=4
Associated Conditions
Child syndrome
Child syndrome
Other Variants in NSDHL
rs104894909 rs104894901 rs104894902 rs104894903 rs104894904 rs104894905 rs137853863 rs121909834 rs121909833 rs375100066
Ask Dr. Hemsworth about this variant