RS104894867 NDP

Health Risk Chr X:43949931 snv missense variant
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What This Variant Does
"[OMIM:?]
Associated Conditions
Atrophia bulborum hereditaria
Hearing impairment
Atrophia bulborum hereditaria
Hearing impairment
Population Frequencies
gnomAD ALL
0%
Other Variants in NDP
rs104894868 rs104894869 rs104894870 rs104894871 rs28933684 rs104894872 rs104894873 rs28933685 rs104894878 rs104894879
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