List of variants in gene DSTYK reported as uncertain significance by GeneDx

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 12

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HGVS	dbSNP	gnomAD frequency
NM_015375.3(DSTYK):c.257T>A (p.Leu86Gln)	rs146982479	0.00034
NM_015375.3(DSTYK):c.1959A>T (p.Lys653Asn)	rs147872876	0.00002
NM_015375.3(DSTYK):c.1489_1491del (p.Arg497del)	rs2102404366
NM_015375.3(DSTYK):c.178A>G (p.Asn60Asp)	rs1659373072
NM_015375.3(DSTYK):c.1802C>T (p.Ala601Val)	rs867889224
NM_015375.3(DSTYK):c.2215C>G (p.Arg739Gly)
NM_015375.3(DSTYK):c.2218G>A (p.Asp740Asn)	rs2102396676
NM_015375.3(DSTYK):c.2258C>T (p.Thr753Ile)	rs2526807549
NM_015375.3(DSTYK):c.265+2T>C
NM_015375.3(DSTYK):c.352G>A (p.Gly118Ser)	rs976476529
NM_015375.3(DSTYK):c.752C>G (p.Ala251Gly)
NM_015375.3(DSTYK):c.971G>A (p.Gly324Asp)	rs765333744

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