ClinVar Miner

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

Included ClinVar conditions (891):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 29
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HGVS dbSNP
NM_207361.5(FREM2):c.*1428A>G rs9548522
NM_207361.5(FREM2):c.*2140C>G rs7324632
NM_207361.5(FREM2):c.*2926G>A rs1945508
NM_207361.5(FREM2):c.*3192T>C rs7337135
NM_207361.5(FREM2):c.*342G>A rs9603463
NM_207361.5(FREM2):c.*3481G>A rs2184141
NM_207361.5(FREM2):c.*4465C>T rs2027770
NM_207361.5(FREM2):c.*4560G>A rs2225623
NM_207361.5(FREM2):c.*4770C>T rs6563648
NM_207361.5(FREM2):c.*5335A>G rs9548524
NM_207361.5(FREM2):c.*5491G>A rs2226913
NM_207361.5(FREM2):c.*5542T>A rs7327529
NM_207361.5(FREM2):c.*5562C>G rs1945507
NM_207361.5(FREM2):c.*5598T>G rs1945506
NM_207361.5(FREM2):c.*5627delT rs5802961
NM_207361.5(FREM2):c.*5733C>T rs1945505
NM_207361.5(FREM2):c.*5899C>T rs1945504
NM_207361.5(FREM2):c.*992T>C rs9532297
NM_207361.5(FREM2):c.1542C>T (p.Ala514=) rs12874397
NM_207361.5(FREM2):c.2233C= (p.Pro745=) rs2496423
NM_207361.5(FREM2):c.2250C>T (p.Asp750=) rs41292755
NM_207361.5(FREM2):c.3209T>C (p.Phe1070Ser) rs2496425
NM_207361.5(FREM2):c.576G>A (p.Glu192=) rs1868464
NM_207361.5(FREM2):c.6196C>T (p.Arg2066Cys) rs9548505
NM_207361.5(FREM2):c.6458C>G (p.Thr2153Ser) rs9548506
NM_207361.5(FREM2):c.6459T>C (p.Thr2153=) rs9548507
NM_207361.5(FREM2):c.6977C>T (p.Thr2326Ile) rs9548509
NM_207361.5(FREM2):c.7398A>G (p.Thr2466=) rs9532292
NM_207361.5(FREM2):c.7984-10G>A rs9532295

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