RS782143078 NSDHL

Health Risk Chr X:152868836
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Associated Conditions
Inborn genetic diseases
Child syndrome
CK syndrome
Thyroid cancer
nonmedullary
1
Inborn genetic diseases
Child syndrome
CK syndrome
Thyroid cancer
nonmedullary
1
Other Variants in NSDHL
rs104894909 rs104894901 rs104894902 rs104894903 rs104894904 rs104894905 rs137853863 rs121909834 rs121909833 rs375100066
Ask Dr. Hemsworth about this variant