RS137853861 GALE

Health Risk Chr 1:23796233 snv missense variant
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What This Variant Does
"[OMIM:?]
Associated Conditions
UDPglucose-4-epimerase deficiency
Thrombocytopenia 13
syndromic
UDPglucose-4-epimerase deficiency
Thrombocytopenia 13
syndromic
Population Frequencies
gnomAD ALL
0%
Other Variants in GALE
rs121908045 rs121908046 rs28940882 rs28940884 rs3180383 rs28940885 rs121908047 rs137853859 rs137853860 rs200584878
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