ClinVar Miner

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

Included ClinVar conditions (962):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 80
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HGVS dbSNP
NM_207361.6(FREM2):c.*1041C>T rs9548521
NM_207361.6(FREM2):c.*1379T>C
NM_207361.6(FREM2):c.*1428A>G rs9548522
NM_207361.6(FREM2):c.*1467G>A rs9548523
NM_207361.6(FREM2):c.*1624G>A rs17443575
NM_207361.6(FREM2):c.*1694A>G rs17443589
NM_207361.6(FREM2):c.*2140C>G rs7324632
NM_207361.6(FREM2):c.*2375C>G rs114706463
NM_207361.6(FREM2):c.*2926G>A rs1945508
NM_207361.6(FREM2):c.*3192T>C rs7337135
NM_207361.6(FREM2):c.*342G>A rs9603463
NM_207361.6(FREM2):c.*3481G>A rs2184141
NM_207361.6(FREM2):c.*3929G>T rs79571295
NM_207361.6(FREM2):c.*4249A>C
NM_207361.6(FREM2):c.*4465C>T rs2027770
NM_207361.6(FREM2):c.*4560G>A rs2225623
NM_207361.6(FREM2):c.*4770C>T rs6563648
NM_207361.6(FREM2):c.*5019A>T rs76274648
NM_207361.6(FREM2):c.*5335A>G rs9548524
NM_207361.6(FREM2):c.*5344T>G
NM_207361.6(FREM2):c.*5491G>A rs2226913
NM_207361.6(FREM2):c.*5542T>A rs7327529
NM_207361.6(FREM2):c.*5562C>G rs1945507
NM_207361.6(FREM2):c.*5598T>G rs1945506
NM_207361.6(FREM2):c.*5600G>T rs74793552
NM_207361.6(FREM2):c.*5612T>G rs200747289
NM_207361.6(FREM2):c.*5627del rs5802961
NM_207361.6(FREM2):c.*5733C>T rs1945505
NM_207361.6(FREM2):c.*5899C>T rs1945504
NM_207361.6(FREM2):c.*992T>C rs9532297
NM_207361.6(FREM2):c.-260A>G rs7997838
NM_207361.6(FREM2):c.1188G>C (p.Gln396His) rs61997174
NM_207361.6(FREM2):c.1518C>T (p.Ser506=) rs141821695
NM_207361.6(FREM2):c.1542C>T (p.Ala514=) rs12874397
NM_207361.6(FREM2):c.176G>A (p.Gly59Asp) rs115327344
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.2180G>A (p.Arg727His) rs201714905
NM_207361.6(FREM2):c.2233= (p.Pro745=) rs2496423
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.2600C>T (p.Thr867Ile) rs61995710
NM_207361.6(FREM2):c.2602C>G (p.Leu868Val) rs7329939
NM_207361.6(FREM2):c.2978A>G (p.Glu993Gly) rs61742843
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.3209T>C (p.Phe1070Ser) rs2496425
NM_207361.6(FREM2):c.3753C>T (p.Ser1251=) rs78099370
NM_207361.6(FREM2):c.3979T>A (p.Leu1327Ile) rs116653247
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.4726C>G (p.Pro1576Ala) rs116742938
NM_207361.6(FREM2):c.4730T>C (p.Ile1577Thr) rs114798977
NM_207361.6(FREM2):c.4901C>T (p.Thr1634Met) rs74781600
NM_207361.6(FREM2):c.4916G>A (p.Arg1639Lys) rs77886481
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.576G>A (p.Glu192=) rs1868464
NM_207361.6(FREM2):c.6036C>T (p.Phe2012=) rs115455037
NM_207361.6(FREM2):c.6196C>T (p.Arg2066Cys) rs9548505
NM_207361.6(FREM2):c.6330T>G (p.Leu2110=) rs112083916
NM_207361.6(FREM2):c.6339C>T (p.Pro2113=) rs116383837
NM_207361.6(FREM2):c.6396C>T (p.Phe2132=) rs61745902
NM_207361.6(FREM2):c.6458C>G (p.Thr2153Ser) rs9548506
NM_207361.6(FREM2):c.6459T>C (p.Thr2153=) rs9548507
NM_207361.6(FREM2):c.6606G>A (p.Glu2202=) rs61749310
NM_207361.6(FREM2):c.6826G>A (p.Val2276Met) rs555028352
NM_207361.6(FREM2):c.6925+7G>T rs79530106
NM_207361.6(FREM2):c.6977C>T (p.Thr2326Ile) rs9548509
NM_207361.6(FREM2):c.6989T>C (p.Val2330Ala) rs61744595
NM_207361.6(FREM2):c.7068C>T (p.Ala2356=) rs74577582
NM_207361.6(FREM2):c.7398A>G (p.Thr2466=) rs9532292
NM_207361.6(FREM2):c.7984-10G>A rs9532295
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.8902G>A (p.Val2968Ile) rs116099212
NM_207361.6(FREM2):c.9184G>T (p.Ala3062Ser) rs140456319
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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