RS121908652 WNT4

Health Risk Chr 1:22129681 snv missense variant
Upload your DNA to see your genotype for this variant.
What This Variant Does
"[OMIM:?]
Associated Conditions
Mullerian aplasia and hyperandrogenism
Mullerian aplasia and hyperandrogenism
Population Frequencies
gnomAD ALL
0%
Other Variants in WNT4
rs121908650 rs121908651 rs121908653 rs368885409 rs150242481
Ask Dr. Hemsworth about this variant