List of variants in gene DST reported as likely pathogenic by Invitae

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: 24

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HGVS	dbSNP	gnomAD frequency
NM_001374736.1(DST):c.16609-1G>T	rs766657292	0.00003
NM_001374736.1(DST):c.11928+1G>A	rs2152697802
NM_001374736.1(DST):c.13236+1G>A
NM_001374736.1(DST):c.16608+1G>A	rs748746313
NM_001374736.1(DST):c.17595+1G>A	rs2096858510
NM_001374736.1(DST):c.17923-2A>G	rs2152506082
NM_001374736.1(DST):c.18577-2del
NM_001374736.1(DST):c.19012+1G>A
NM_001374736.1(DST):c.19464+1G>A
NM_001374736.1(DST):c.19567-29_19570del
NM_001374736.1(DST):c.20757+1G>A	rs2152440123
NM_001374736.1(DST):c.21048-1G>T	rs2152427474
NM_001374736.1(DST):c.21208-2A>T	rs2152422891
NM_001374736.1(DST):c.21403-1G>A
NM_001374736.1(DST):c.22476+1G>A	rs2152394710
NM_001374736.1(DST):c.22569+2T>C
NM_001374736.1(DST):c.22959+1G>A	rs2094441686
NM_001374736.1(DST):c.22960-2A>C
NM_001374736.1(DST):c.23071-2A>G	rs2152370482
NM_001374736.1(DST):c.2619+1G>A
NM_001374736.1(DST):c.3061-2A>T	rs1454639285
NM_001374736.1(DST):c.3187-2A>G	rs200803122
NM_001374736.1(DST):c.4278_4281+1del
NM_001374736.1(DST):c.4281+1G>A	rs1587154269

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