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

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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: 42

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HGVS	dbSNP	gnomAD frequency
NM_000169.3(GLA):c.-12G>A	rs3027585	0.06554
NM_000169.3(GLA):c.-10C>T	rs2071225	0.06441
NM_000169.3(GLA):c.640-532G>A	rs143833648	0.00740
NM_000169.3(GLA):c.640-749C>T	rs148135742	0.00529
NM_000169.3(GLA):c.369+163A>G	rs370226383	0.00524
NM_000169.3(GLA):c.937G>T (p.Asp313Tyr)	rs28935490	0.00308
NM_001199973.2(RPL36A-HNRNPH2):c.300+2303T>C	rs191249601	0.00265
NM_000169.3(GLA):c.640-607G>T	rs185121865	0.00102
NM_000169.3(GLA):c.978G>A (p.Lys326=)	rs151195362	0.00100
NM_000169.3(GLA):c.639+18G>A	rs189319122	0.00087
NM_000169.3(GLA):c.376A>G (p.Ser126Gly)	rs149391489	0.00043
NM_000169.3(GLA):c.352C>T (p.Arg118Cys)	rs148158093	0.00040
NM_000169.3(GLA):c.427G>A (p.Ala143Thr)	rs104894845	0.00039
NM_000169.3(GLA):c.-44C>T	rs781906252	0.00025
NM_000169.3(GLA):c.195-1193C>T	rs887996815	0.00023
NM_000169.3(GLA):c.129C>T (p.Gly43=)	rs146177035	0.00018
NM_000169.3(GLA):c.123C>T (p.Thr41=)	rs137902198	0.00017
NM_000169.3(GLA):c.48T>G (p.Leu16=)	rs201449986	0.00011
NM_000169.3(GLA):c.865A>G (p.Ile289Val)	rs140329381	0.00009
NM_000169.3(GLA):c.945C>T (p.Asp315=)	rs151208856	0.00009
NM_000169.3(GLA):c.639+796C>A	rs184705124	0.00004
NM_000169.3(GLA):c.416A>G (p.Asn139Ser)	rs138886989	0.00003
NM_000169.3(GLA):c.195T>C (p.Ser65=)	rs782803696	0.00002
NM_000169.3(GLA):c.1008C>T (p.Asn336=)	rs901454780	0.00001
NM_000169.3(GLA):c.1153A>G (p.Thr385Ala)	rs397515869	0.00001
NM_000169.3(GLA):c.247G>A (p.Asp83Asn)	rs782722577	0.00001
NM_000169.3(GLA):c.640-11T>C	rs782634293	0.00001
NM_000169.2(GLA):c.-24T>G	rs1603048396
NM_000169.3(GLA):c.1290A>G (p.Ter430=)	rs1555984712
NM_000169.3(GLA):c.194+229TC[17]	rs782246787
NM_000169.3(GLA):c.194+229TC[21]	rs782246787
NM_000169.3(GLA):c.194+229TC[23]	rs782246787
NM_000169.3(GLA):c.195-1144C>T
NM_000169.3(GLA):c.195-1236T>C
NM_000169.3(GLA):c.525C>G (p.Asp175Glu)	rs782722844
NM_000169.3(GLA):c.547+163AATT[3]	rs200739167
NM_000169.3(GLA):c.639+858C>G	rs1603040086
NM_000169.3(GLA):c.70T>A (p.Trp24Arg)	rs397515871
NM_000169.3(GLA):c.88A>C (p.Arg30=)	rs1603047946
NM_000169.3(GLA):c.921C>G (p.Ala307=)	rs2147472055
NM_000169.3(GLA):c.937G>A (p.Asp313Asn)	rs28935490
NM_001199973.2(RPL36A-HNRNPH2):c.300+2092C>T	rs140006150

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