List of variants in gene GSN reported as 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.1417-22T>C	rs306769	0.85170
NM_198252.3(GSN):c.1763-34G>A	rs306771	0.80923
NM_198252.3(GSN):c.2115T>C (p.Phe705=)	rs9102	0.07073
NM_198252.3(GSN):c.1694C>T (p.Thr565Met)	rs76463933	0.05893
NM_198252.3(GSN):c.1260C>T (p.Gly420=)	rs2304393	0.05790
NM_198252.3(GSN):c.232G>A (p.Ala78Thr)	rs2230287	0.03231
NM_198252.3(GSN):c.1535C>G (p.Thr512Ser)	rs77681311	0.02987
NM_198252.3(GSN):c.29A>G (p.Lys10Arg)	rs115224458	0.02654
NM_198252.3(GSN):c.538A>G (p.Asn180Asp)	rs11550199	0.01287
NM_198252.3(GSN):c.1239A>G (p.Thr413=)	rs149375418	0.00861
NM_198252.3(GSN):c.382G>A (p.Val128Met)	rs41305623	0.00507
NM_198252.3(GSN):c.196+7C>T	rs146379508	0.00444
NM_198252.3(GSN):c.1680C>T (p.Ser560=)	rs73660439	0.00379
NM_198252.3(GSN):c.664-4A>G	rs143590302	0.00376
NM_198252.3(GSN):c.1850G>T (p.Arg617Leu)	rs9696578	0.00359
NM_198252.3(GSN):c.1288C>T (p.Arg430Cys)	rs116185403	0.00357
NM_198252.3(GSN):c.243C>T (p.Thr81=)	rs116956127	0.00302
NM_198252.3(GSN):c.1225G>A (p.Val409Met)	rs140042418	0.00103
NM_198252.3(GSN):c.1663G>A (p.Val555Met)	rs151208452	0.00063
NM_198252.3(GSN):c.1555G>A (p.Ala519Thr)	rs147554026	0.00058
NM_198252.3(GSN):c.1931C>T (p.Thr644Met)	rs144434647	0.00057
NM_198252.3(GSN):c.271C>T (p.Arg91Trp)	rs146956976	0.00041
NM_198252.3(GSN):c.1513G>A (p.Gly505Arg)	rs58750568	0.00033
NM_198252.3(GSN):c.2069G>A (p.Arg690Gln)	rs141510612	0.00029
NM_198252.3(GSN):c.1563C>T (p.Ser521=)	rs140414249	0.00026
NM_198252.3(GSN):c.1098G>A (p.Val366=)	rs201325199	0.00025
NM_198252.3(GSN):c.1487A>G (p.Tyr496Cys)	rs139832048	0.00025
NM_198252.3(GSN):c.-9-1967C>T	rs372837702	0.00020
NM_198252.3(GSN):c.1421G>A (p.Arg474His)	rs142828669	0.00019
NM_198252.3(GSN):c.1727C>G (p.Ala576Gly)	rs567372749	0.00016
NM_198252.3(GSN):c.754-11C>T	rs374057474	0.00016
NM_198252.3(GSN):c.1191+4C>T	rs372713895	0.00014
NM_198252.3(GSN):c.1170C>T (p.Asp390=)	rs147583697	0.00013
NM_198252.3(GSN):c.1782G>A (p.Leu594=)	rs139239940	0.00012
NM_198252.3(GSN):c.2046G>A (p.Thr682=)	rs747385746	0.00011
NM_198252.3(GSN):c.547C>T (p.Arg183Trp)	rs371175865	0.00007
NM_198252.3(GSN):c.1191+14G>A	rs377308627	0.00006
NM_198252.3(GSN):c.1423G>T (p.Val475Leu)	rs766945413	0.00005
NM_198252.3(GSN):c.1443C>T (p.Pro481=)	rs200156774	0.00003
NM_198252.3(GSN):c.1009C>T (p.Leu337=)	rs528161256	0.00001
NM_198252.3(GSN):c.163G>A (p.Gly55Arg)	rs556563870	0.00001
NM_198252.3(GSN):c.1874T>C (p.Ile625Thr)	rs777767455	0.00001
NM_198252.3(GSN):c.1171G>A (p.Asp391Asn)	rs142034230
NM_198252.3(GSN):c.231C>A (p.Ala77=)	rs140734150

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