List of variants reported as benign for pulmonary fibrosis and/or bone marrow failure, Telomere-related, 4

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Total variants: 25

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HGVS	dbSNP	gnomAD frequency
NM_002582.4(PARN):c.918+14T>C	rs75783314	0.04521
NM_002582.4(PARN):c.1383T>C (p.Leu461=)	rs143472178	0.00920
NM_002582.4(PARN):c.1690G>A (p.Val564Ile)	rs35722504	0.00623
NM_002582.4(PARN):c.840+6del	rs531994703	0.00452
NM_002582.4(PARN):c.840+6T>C	rs59687658	0.00184
NM_002582.4(PARN):c.1741G>A (p.Gly581Arg)	rs75007073	0.00146
NM_002582.4(PARN):c.1761C>T (p.Ser587=)	rs148052946	0.00110
NM_002582.4(PARN):c.1263-8T>G	rs182460499	0.00097
NM_002582.4(PARN):c.825C>T (p.His275=)	rs374114285	0.00073
NM_002582.4(PARN):c.1102A>T (p.Ser368Cys)	rs138984302	0.00050
NM_002582.4(PARN):c.1843A>G (p.Lys615Glu)	rs368440052	0.00046
NM_002582.4(PARN):c.1006-5T>C	rs377692519	0.00026
NM_002582.4(PARN):c.1192+4C>T	rs185546844	0.00018
NM_002582.4(PARN):c.978A>G (p.Lys326=)	rs200678657	0.00017
NM_002582.4(PARN):c.1082-13T>A	rs188469919	0.00006
NM_002582.4(PARN):c.1006-12C>T	rs767292858	0.00002
NM_002582.4(PARN):c.1082-6dup	rs763461320
NM_002582.4(PARN):c.1192+5G>A
NM_002582.4(PARN):c.1193-10del
NM_002582.4(PARN):c.1481-14del	rs748039977
NM_002582.4(PARN):c.1670+17G>T	rs116427010
NM_002582.4(PARN):c.245+20G>A	rs377105548
NM_002582.4(PARN):c.703-3dup
NM_002582.4(PARN):c.919-3T>C	rs2151757180
NM_002582.4(PARN):c.963-11del	rs756034248

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