List of variants in gene SLCO2A1 studied for Hypertrophic osteoarthropathy, primary, autosomal dominant

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Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 8

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HGVS	dbSNP	gnomAD frequency
NM_005630.3(SLCO2A1):c.234+45G>C	rs4640563	0.88709
NM_005630.3(SLCO2A1):c.397+10T>C	rs4634113	0.87506
NM_005630.3(SLCO2A1):c.1807C>T (p.Arg603Ter)	rs776813259	0.00004
NM_005630.3(SLCO2A1):c.1660G>A (p.Gly554Arg)	rs1177054873	0.00001
NM_005630.3(SLCO2A1):c.302T>G (p.Ile101Ser)	rs765824772
NM_005630.3(SLCO2A1):c.310G>T (p.Gly104Ter)	rs387907297
NM_005630.3(SLCO2A1):c.664G>A (p.Gly222Arg)	rs774795340
NM_005630.3(SLCO2A1):c.861+2T>C	rs2108043577

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