ClinVar Miner

List of variants in gene FREM2 reported as likely benign for abdominal and pelvic region disorder

Included ClinVar conditions (902):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 33
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HGVS dbSNP
NM_207361.5(FREM2):c.7520-5delT rs36084034
NM_207361.6(FREM2):c.*1041C>T rs9548521
NM_207361.6(FREM2):c.*1467G>A rs9548523
NM_207361.6(FREM2):c.*2375C>G rs114706463
NM_207361.6(FREM2):c.*2390_*2392del rs149897768
NM_207361.6(FREM2):c.*3929G>T rs79571295
NM_207361.6(FREM2):c.*5019A>T rs76274648
NM_207361.6(FREM2):c.*5600G>T rs74793552
NM_207361.6(FREM2):c.*5612T>G rs200747289
NM_207361.6(FREM2):c.-260A>G rs7997838
NM_207361.6(FREM2):c.1518C>T (p.Ser506=) rs141821695
NM_207361.6(FREM2):c.1941C>T (p.Asp647=) rs41292751
NM_207361.6(FREM2):c.2165G>A (p.Arg722Lys) rs58363253
NM_207361.6(FREM2):c.2250C>T (p.Asp750=) rs41292755
NM_207361.6(FREM2):c.2308G>A (p.Val770Met) rs7327915
NM_207361.6(FREM2):c.2602C>G (p.Leu868Val) rs7329939
NM_207361.6(FREM2):c.303C>A (p.Pro101=) rs8002488
NM_207361.6(FREM2):c.3116T>A (p.Met1039Lys) rs2496424
NM_207361.6(FREM2):c.3753C>T (p.Ser1251=) rs78099370
NM_207361.6(FREM2):c.4077T>A (p.Gly1359=) rs41292757
NM_207361.6(FREM2):c.4686T>C (p.Asp1562=) rs17058435
NM_207361.6(FREM2):c.4901C>T (p.Thr1634Met) rs74781600
NM_207361.6(FREM2):c.5003G>A (p.Arg1668His) rs1868463
NM_207361.6(FREM2):c.5518C>T (p.Arg1840Trp) rs9603422
NM_207361.6(FREM2):c.6036C>T (p.Phe2012=) rs115455037
NM_207361.6(FREM2):c.6339C>T (p.Pro2113=) rs116383837
NM_207361.6(FREM2):c.6606G>A (p.Glu2202=) rs61749310
NM_207361.6(FREM2):c.6925+7G>T rs79530106
NM_207361.6(FREM2):c.8226C>T (p.Ala2742=) rs17058710
NM_207361.6(FREM2):c.8885C>T (p.Ala2962Val) rs7996253
NM_207361.6(FREM2):c.9357G>C (p.Thr3119=) rs41306664
NM_207361.6(FREM2):c.9429G>A (p.Gly3143=) rs41306662
NM_207361.6(FREM2):c.954C>G (p.Pro318=) rs9576597

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