ClinVar Miner

List of variants in gene FREM2 reported as likely benign by CeGaT Center for Human Genetics Tuebingen

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Gene type:
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Total variants: 21
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HGVS dbSNP gnomAD frequency
NM_207361.6(FREM2):c.1518C>T (p.Ser506=) rs141821695 0.00784
NM_207361.6(FREM2):c.4031G>A (p.Arg1344His) rs143044921 0.00430
NM_207361.6(FREM2):c.3979T>A (p.Leu1327Ile) rs116653247 0.00384
NM_207361.6(FREM2):c.8902G>A (p.Val2968Ile) rs116099212 0.00379
NM_207361.6(FREM2):c.8460C>G (p.Ala2820=) rs138775857 0.00325
NM_207361.6(FREM2):c.84C>G (p.Pro28=) rs141718695 0.00194
NM_207361.6(FREM2):c.7323G>A (p.Ala2441=) rs147563277 0.00155
NM_207361.6(FREM2):c.9038C>T (p.Thr3013Met) rs114400765 0.00118
NM_207361.6(FREM2):c.7429C>T (p.Arg2477Trp) rs143571375 0.00115
NM_207361.6(FREM2):c.5417G>A (p.Gly1806Asp) rs145208009 0.00101
NM_207361.6(FREM2):c.109C>T (p.Leu37Phe) rs183560588 0.00081
NM_207361.6(FREM2):c.2754C>T (p.Val918=) rs140353326 0.00046
NM_207361.6(FREM2):c.4960A>C (p.Ser1654Arg) rs114595447 0.00046
NM_207361.6(FREM2):c.7062G>A (p.Thr2354=) rs41286130 0.00026
NM_207361.6(FREM2):c.1737C>T (p.Ile579=) rs144811771 0.00012
NM_207361.6(FREM2):c.6465T>C (p.Asp2155=) rs373878188 0.00005
NM_207361.6(FREM2):c.2062C>G (p.Arg688Gly) rs150928081
NM_207361.6(FREM2):c.3677C>G (p.Thr1226Ser)
NM_207361.6(FREM2):c.3729A>C (p.Ile1243=) rs1306457101
NM_207361.6(FREM2):c.7209T>C (p.Cys2403=)
NM_207361.6(FREM2):c.7663G>T (p.Val2555Leu) rs200997496

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