RS132630327 NR0B1

Health Risk Chr X:30309049
Upload your DNA to see your genotype for this variant.
What This Variant Does
"[OMIM:?]
Associated Conditions
Mineralocorticoid deficiency
isolated
Congenital adrenal hypoplasia
X-linked
46
XY sex reversal 2
Congenital adrenal hypoplasia
X-linked
Mineralocorticoid deficiency
isolated
Congenital adrenal hypoplasia
X-linked
46
XY sex reversal 2
Congenital adrenal hypoplasia
Other Variants in NR0B1
rs104894890 rs104894886 rs104894887 rs104894888 rs104894889 rs104894891 rs2519051116 rs104894892 rs28935481 rs104894894
Ask Dr. Hemsworth about this variant