List of variants in gene GSN reported as likely benign for corneal disorder

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: 44

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HGVS	dbSNP	gnomAD frequency
NM_198252.3(GSN):c.513+19T>C	rs79969850	0.00853
NM_198252.3(GSN):c.664-4A>G	rs143590302	0.00376
NM_198252.3(GSN):c.243C>T (p.Thr81=)	rs116956127	0.00302
NM_198252.3(GSN):c.597C>T (p.Asn199=)	rs146329975	0.00258
NM_198252.3(GSN):c.1416+16C>T	rs116723395	0.00233
NM_198252.3(GSN):c.186C>T (p.His62=)	rs144551136	0.00175
NM_198252.3(GSN):c.886+19G>T	rs200255784	0.00159
NM_198252.3(GSN):c.1637A>G (p.Lys546Arg)	rs184844415	0.00086
NM_198252.3(GSN):c.197-4G>A	rs375172023	0.00034
NM_198252.3(GSN):c.1563C>T (p.Ser521=)	rs140414249	0.00026
NM_198252.3(GSN):c.285C>T (p.His95=)	rs142155964	0.00026
NM_198252.3(GSN):c.1325+14G>A	rs113863232	0.00021
NM_198252.3(GSN):c.-9-1943G>A	rs568885924	0.00020
NM_198252.3(GSN):c.1782G>A (p.Leu594=)	rs139239940	0.00012
NM_198252.3(GSN):c.431G>A (p.Arg144Gln)	rs144099356	0.00012
NM_198252.3(GSN):c.2046G>A (p.Thr682=)	rs747385746	0.00011
NM_198252.3(GSN):c.2082C>T (p.Thr694=)	rs368986042	0.00011
NM_198252.3(GSN):c.276C>T (p.Ala92=)	rs548138013	0.00009
NM_198252.3(GSN):c.303C>T (p.Phe101=)	rs373779982	0.00009
NM_198252.3(GSN):c.741C>T (p.Ala247=)	rs751823302	0.00009
NM_198252.3(GSN):c.-9-1951G>T	rs772288409	0.00007
NM_198252.3(GSN):c.126C>T (p.Asp42=)	rs200027070	0.00007
NM_198252.3(GSN):c.1485C>T (p.Ile495=)	rs374982895	0.00007
NM_198252.3(GSN):c.1191+14G>A	rs377308627	0.00006
NM_198252.3(GSN):c.427G>A (p.Gly143Arg)	rs750132751	0.00006
NM_198252.3(GSN):c.1416+17G>A	rs747631468	0.00004
NM_198252.3(GSN):c.2045C>T (p.Thr682Met)	rs142854368	0.00004
NM_198252.3(GSN):c.754-8C>T	rs757725237	0.00004
NM_198252.3(GSN):c.886+10A>G	rs768148669	0.00004
NM_198252.3(GSN):c.1932G>A (p.Thr644=)	rs759980004	0.00003
NM_198252.3(GSN):c.2040C>T (p.Ile680=)	rs758909359	0.00002
NM_198252.3(GSN):c.723G>A (p.Ala241=)	rs377624593	0.00002
NM_198252.3(GSN):c.1009C>T (p.Leu337=)	rs528161256	0.00001
NM_198252.3(GSN):c.123C>T (p.Gly41=)	rs774617795	0.00001
NM_198252.3(GSN):c.1651G>A (p.Ala551Thr)	rs777955781	0.00001
NM_198252.3(GSN):c.1763-10C>T	rs750829888	0.00001
NM_198252.3(GSN):c.2060G>A (p.Arg687Gln)	rs770023727	0.00001
NM_198252.3(GSN):c.393C>T (p.Asn131=)	rs186654124	0.00001
NM_198252.3(GSN):c.-9-1942G>A	rs1268467289
NM_198252.3(GSN):c.1577G>A (p.Arg526Gln)	rs528604896
NM_198252.3(GSN):c.1762+19G>A	rs1274106245
NM_198252.3(GSN):c.1762+20del	rs895358104
NM_198252.3(GSN):c.1887+11G>T	rs147527479
NM_198252.3(GSN):c.886+19G>A	rs200255784

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