RS104894897 NR0B1

Health Risk Chr X:30304676
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What This Variant Does
"[OMIM:?]
Associated Conditions
Congenital adrenal hypoplasia
X-linked
Congenital adrenal hypoplasia
X-linked
Other Variants in NR0B1
rs104894890 rs104894886 rs104894887 rs104894888 rs104894889 rs104894891 rs2519051116 rs104894892 rs28935481 rs104894894
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