List of variants in gene DSC2 reported as benign by Ambry Genetics

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: 19

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HGVS	dbSNP	gnomAD frequency
NM_024422.6(DSC2):c.2326A>G (p.Ile776Val)	rs1893963	0.18480
NM_024422.6(DSC2):c.111A>G (p.Leu37=)	rs12954874	0.10312
NM_024422.6(DSC2):c.351A>G (p.Thr117=)	rs117812913	0.00832
NM_024422.6(DSC2):c.1719C>T (p.Asn573=)	rs140167653	0.00590
NM_024422.6(DSC2):c.1264-5C>T	rs183614856	0.00292
NM_024422.6(DSC2):c.1729A>G (p.Ile577Val)	rs201845641	0.00025
NM_024422.6(DSC2):c.857G>T (p.Gly286Val)	rs199682735	0.00024
NM_024422.6(DSC2):c.2471C>T (p.Ser824Leu)	rs143413607	0.00016
NM_024422.6(DSC2):c.734A>C (p.Glu245Ala)	rs373201722	0.00013
NM_024422.6(DSC2):c.1070G>A (p.Arg357His)	rs201201194	0.00011
NM_024422.6(DSC2):c.2314G>A (p.Val772Met)	rs146029947	0.00010
NM_024422.6(DSC2):c.2151G>C (p.Gly717=)	rs752691135	0.00006
NM_024422.6(DSC2):c.2208C>T (p.Asn736=)	rs727504534	0.00004
NM_024422.6(DSC2):c.408A>G (p.Arg136=)	rs561653481	0.00004
NM_024422.6(DSC2):c.1264-4G>A	rs377439942	0.00003
NM_024422.6(DSC2):c.2393G>A (p.Arg798Gln)	rs61731921
NM_024422.6(DSC2):c.2686_2687dup (p.Ala897fs)	rs200056085
NM_024422.6(DSC2):c.370C>T (p.His124Tyr)	rs371443698
NM_024422.6(DSC2):c.942+13_942+15dup	rs5823783

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