ClinVar Miner

List of variants in gene PARN reported as benign for pulmonary fibrosis

Included ClinVar conditions (20):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
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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