ClinVar Miner

List of variants in gene GSN reported as likely benign for Finnish type amyloidosis

Included ClinVar conditions (1):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 44
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HGVS dbSNP gnomAD frequency
NM_198252.3(GSN):c.513+19T>C rs79969850 0.00853
NM_198252.3(GSN):c.664-4A>G rs143590302 0.00376
NM_198252.3(GSN):c.243C>T (p.Thr81=) rs116956127 0.00302
NM_198252.3(GSN):c.597C>T (p.Asn199=) rs146329975 0.00258
NM_198252.3(GSN):c.1416+16C>T rs116723395 0.00233
NM_198252.3(GSN):c.186C>T (p.His62=) rs144551136 0.00175
NM_198252.3(GSN):c.886+19G>T rs200255784 0.00159
NM_198252.3(GSN):c.1637A>G (p.Lys546Arg) rs184844415 0.00086
NM_198252.3(GSN):c.197-4G>A rs375172023 0.00034
NM_198252.3(GSN):c.1563C>T (p.Ser521=) rs140414249 0.00026
NM_198252.3(GSN):c.285C>T (p.His95=) rs142155964 0.00026
NM_198252.3(GSN):c.1325+14G>A rs113863232 0.00021
NM_198252.3(GSN):c.-9-1943G>A rs568885924 0.00020
NM_198252.3(GSN):c.1782G>A (p.Leu594=) rs139239940 0.00012
NM_198252.3(GSN):c.431G>A (p.Arg144Gln) rs144099356 0.00012
NM_198252.3(GSN):c.2046G>A (p.Thr682=) rs747385746 0.00011
NM_198252.3(GSN):c.2082C>T (p.Thr694=) rs368986042 0.00011
NM_198252.3(GSN):c.276C>T (p.Ala92=) rs548138013 0.00009
NM_198252.3(GSN):c.303C>T (p.Phe101=) rs373779982 0.00009
NM_198252.3(GSN):c.741C>T (p.Ala247=) rs751823302 0.00009
NM_198252.3(GSN):c.-9-1951G>T rs772288409 0.00007
NM_198252.3(GSN):c.126C>T (p.Asp42=) rs200027070 0.00007
NM_198252.3(GSN):c.1485C>T (p.Ile495=) rs374982895 0.00007
NM_198252.3(GSN):c.1191+14G>A rs377308627 0.00006
NM_198252.3(GSN):c.427G>A (p.Gly143Arg) rs750132751 0.00006
NM_198252.3(GSN):c.1416+17G>A rs747631468 0.00004
NM_198252.3(GSN):c.2045C>T (p.Thr682Met) rs142854368 0.00004
NM_198252.3(GSN):c.754-8C>T rs757725237 0.00004
NM_198252.3(GSN):c.886+10A>G rs768148669 0.00004
NM_198252.3(GSN):c.1932G>A (p.Thr644=) rs759980004 0.00003
NM_198252.3(GSN):c.2040C>T (p.Ile680=) rs758909359 0.00002
NM_198252.3(GSN):c.723G>A (p.Ala241=) rs377624593 0.00002
NM_198252.3(GSN):c.1009C>T (p.Leu337=) rs528161256 0.00001
NM_198252.3(GSN):c.123C>T (p.Gly41=) rs774617795 0.00001
NM_198252.3(GSN):c.1651G>A (p.Ala551Thr) rs777955781 0.00001
NM_198252.3(GSN):c.1763-10C>T rs750829888 0.00001
NM_198252.3(GSN):c.2060G>A (p.Arg687Gln) rs770023727 0.00001
NM_198252.3(GSN):c.393C>T (p.Asn131=) rs186654124 0.00001
NM_198252.3(GSN):c.-9-1942G>A rs1268467289
NM_198252.3(GSN):c.1577G>A (p.Arg526Gln) rs528604896
NM_198252.3(GSN):c.1762+19G>A rs1274106245
NM_198252.3(GSN):c.1762+20del rs895358104
NM_198252.3(GSN):c.1887+11G>T rs147527479
NM_198252.3(GSN):c.886+19G>A rs200255784

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