List of variants in gene SSBP1 studied for optic atrophy

Minimum submission review status:		Collection method:
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Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 4

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HGVS	dbSNP	gnomAD frequency
NM_003143.3(SSBP1):c.113G>A (p.Arg38Gln)	rs1799652893
NM_003143.3(SSBP1):c.119G>T (p.Gly40Val)	rs1799653139
NM_003143.3(SSBP1):c.320G>A (p.Arg107Gln)	rs1799747454
NM_003143.3(SSBP1):c.422G>A (p.Ser141Asn)	rs1799915649

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