List of variants in gene combination ASTN2, TRIM32 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: 18

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HGVS	dbSNP	gnomAD frequency
NM_012210.4(TRIM32):c.292C>A (p.Leu98Ile)	rs201877419	0.00039
NM_012210.4(TRIM32):c.521C>T (p.Ser174Phe)	rs138699534	0.00019
NM_012210.4(TRIM32):c.979A>G (p.Met327Val)	rs373287765	0.00009
NM_012210.4(TRIM32):c.1012G>A (p.Ala338Thr)	rs141806013	0.00008
NM_012210.4(TRIM32):c.1223G>A (p.Arg408His)	rs183136193	0.00006
NM_012210.4(TRIM32):c.480G>A (p.Met160Ile)	rs200196832	0.00006
NM_012210.4(TRIM32):c.1168C>T (p.Arg390Cys)	rs754554333	0.00003
NM_012210.4(TRIM32):c.1930A>G (p.Ser644Gly)	rs1462453134	0.00003
NM_012210.4(TRIM32):c.370C>T (p.Arg124Trp)	rs572052810	0.00002
NM_012210.4(TRIM32):c.712C>T (p.Arg238Cys)	rs769410403	0.00002
GRCh37/hg19 9q33.1(chr9:119449044-119952215)x1
NM_012210.4(TRIM32):c.112C>T (p.His38Tyr)	rs2132070294
NM_012210.4(TRIM32):c.1143T>G (p.Ser381Arg)	rs1861027670
NM_012210.4(TRIM32):c.1472G>T (p.Gly491Val)
NM_012210.4(TRIM32):c.1786C>G (p.Arg596Gly)	rs765348678
NM_012210.4(TRIM32):c.40C>G (p.Leu14Val)	rs756350336
NM_012210.4(TRIM32):c.479T>C (p.Met160Thr)	rs199699832
NM_012210.4(TRIM32):c.811C>T (p.Arg271Trp)	rs372298402

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