List of variants in gene combination GLA, RPL36A-HNRNPH2 reported as likely benign for not specified

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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: 39

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HGVS	dbSNP	gnomAD frequency
NM_000169.3(GLA):c.937G>T (p.Asp313Tyr)	rs28935490	0.00308
NM_000169.3(GLA):c.640-731G>A	rs2473815	0.00218
NM_000169.3(GLA):c.978G>A (p.Lys326=)	rs151195362	0.00100
NM_000169.3(GLA):c.8T>C (p.Leu3Pro)	rs150547672	0.00098
NM_000169.3(GLA):c.376A>G (p.Ser126Gly)	rs149391489	0.00043
NM_000169.3(GLA):c.129C>T (p.Gly43=)	rs146177035	0.00018
NM_000169.3(GLA):c.-8C>G	rs371291716	0.00014
NM_000169.3(GLA):c.48T>G (p.Leu16=)	rs201449986	0.00011
NM_000169.3(GLA):c.945C>T (p.Asp315=)	rs151208856	0.00009
NM_000169.2(GLA):c.-32G>A	rs1057523740	0.00005
NM_000169.3(GLA):c.-13G>C	rs782051708	0.00004
NM_000169.3(GLA):c.1000-14T>C	rs397515868	0.00004
NM_000169.3(GLA):c.1261A>G (p.Met421Val)	rs144060196	0.00004
NM_000169.3(GLA):c.6G>A (p.Gln2=)	rs782748047	0.00004
NM_000169.3(GLA):c.416A>G (p.Asn139Ser)	rs138886989	0.00003
NM_000169.3(GLA):c.639+6A>C	rs200096940	0.00003
NM_000169.3(GLA):c.714T>C (p.Ser238=)	rs397515872	0.00003
NM_000169.3(GLA):c.196G>C (p.Glu66Gln)	rs104894833	0.00002
NM_000169.3(GLA):c.320A>G (p.Gln107Arg)	rs727505060	0.00002
NM_000169.3(GLA):c.501A>T (p.Leu167=)	rs782486830	0.00002
NM_000169.3(GLA):c.984G>T (p.Gly328=)	rs376623208	0.00002
NM_000169.3(GLA):c.991C>T (p.Leu331Phe)	rs730880437	0.00002
NM_000169.3(GLA):c.1008C>T (p.Asn336=)	rs901454780	0.00001
NM_000169.3(GLA):c.1050T>C (p.Ala350=)	rs869312210	0.00001
NM_000169.3(GLA):c.1095T>C (p.Tyr365=)	rs104894849	0.00001
NM_000169.3(GLA):c.1153A>G (p.Thr385Ala)	rs397515869	0.00001
NM_000169.3(GLA):c.1191T>C (p.Tyr397=)	rs869312236	0.00001
NM_000169.3(GLA):c.1233C>T (p.Gly411=)	rs1555984746	0.00001
NM_000169.3(GLA):c.133C>T (p.Leu45=)	rs143084761	0.00001
NM_000169.3(GLA):c.345T>C (p.His115=)	rs782260908	0.00001
NM_000169.3(GLA):c.801+14C>T	rs200744672	0.00001
NM_000169.2(GLA):c.-44C>G	rs781906252
NM_000169.3(GLA):c.1102G>A (p.Ala368Thr)	rs144994244
NM_000169.3(GLA):c.1102G>C (p.Ala368Pro)	rs144994244
NM_000169.3(GLA):c.194+14G>C	rs876657469
NM_000169.3(GLA):c.28C>T (p.Leu10=)	rs727503073
NM_000169.3(GLA):c.591C>T (p.Ser197=)	rs898606246
NM_000169.3(GLA):c.630C>T (p.Pro210=)	rs727503071
NM_000169.3(GLA):c.721A>G (p.Ser241Gly)	rs730880438

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