List of variants in gene combination ASTN2, TRIM32 reported as benign for autosomal recessive limb-girdle muscular dystrophy type 2H

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

Total variants: 6

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HGVS	dbSNP	gnomAD frequency
NM_012210.4(TRIM32):c.*129C>T	rs3019	0.93964
NM_012210.4(TRIM32):c.*1206T>C	rs2281627	0.28741
NM_012210.4(TRIM32):c.-133G>C	rs12342207	0.27173
NM_012210.4(TRIM32):c.1254G>A (p.Val418=)	rs1661300	0.10569
NM_012210.4(TRIM32):c.*589G>A	rs16933835	0.01666
NM_012210.4(TRIM32):c.*845C>T	rs111309723	0.01665

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