List of variants in gene SEPSECS reported as likely benign for Pontocerebellar hypoplasia type 2D

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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: 8

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HGVS	dbSNP	gnomAD frequency
NM_016955.4(SEPSECS):c.*455C>T	rs73252520	0.08857
NM_016955.4(SEPSECS):c.*2694A>G	rs956925	0.07936
NM_016955.4(SEPSECS):c.*638G>C	rs10004441	0.01839
NM_016955.4(SEPSECS):c.*2209A>G	rs9998044	0.01837
NM_016955.4(SEPSECS):c.*1041T>C	rs114420733	0.01027
NM_016955.4(SEPSECS):c.*3402A>G	rs149506792	0.00300
NM_016955.4(SEPSECS):c.780A>G (p.Ser260=)	rs61747281	0.00120
NM_016955.4(SEPSECS):c.45G>A (p.Pro15=)	rs77226826	0.00014

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