RS28935481 NR0B1

Health Risk Chr X:30304673
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What This Variant Does
"[OMIM:ADRENAL HYPOPLASIA, CONGENITAL]
Associated Conditions
Congenital adrenal hypoplasia
X-linked
Congenital adrenal hypoplasia
X-linked
Other Variants in NR0B1
rs104894890 rs104894886 rs104894887 rs104894888 rs104894889 rs104894891 rs2519051116 rs104894892 rs104894894 rs104894895
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