RS121912583 SLC29A3

Health Risk Chr 10:71362458 snv missense variant
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What This Variant Does
"[OMIM:?]
Associated Conditions
H syndrome
H syndrome
Population Frequencies
gnomAD ALL
0%
Other Variants in SLC29A3
rs780668 rs267607056 rs121912584 rs869025176 rs869025177 rs267607057 rs267607058 rs796052139 rs387907066 rs387907067
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