ClinVar Miner

List of variants reported as uncertain significance for anterior segment dysgenesis 3

Included ClinVar conditions (3):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 14
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HGVS dbSNP
NM_001453.3(FOXC1):c.1051G>C (p.Gly351Arg) rs897755884
NM_001453.3(FOXC1):c.1064C>T (p.Pro355Leu) rs886043447
NM_001453.3(FOXC1):c.1154G>A (p.Gly385Glu) rs1215019381
NM_001453.3(FOXC1):c.1370A>G (p.Gln457Arg)
NM_001453.3(FOXC1):c.235C>T (p.Pro79Ser) rs1554100945
NM_001453.3(FOXC1):c.268G>A (p.Ala90Thr) rs1057519473
NM_001453.3(FOXC1):c.269C>A (p.Ala90Asp) rs1057519474
NM_001453.3(FOXC1):c.344A>G (p.Tyr115Cys)
NM_001453.3(FOXC1):c.356A>G (p.Lys119Arg) rs759264099
NM_001453.3(FOXC1):c.457A>C (p.Thr153Pro) rs1057519476
NM_001453.3(FOXC1):c.486C>G (p.Phe162Leu)
NM_001453.3(FOXC1):c.508C>T (p.Arg170Trp)
NM_001453.3(FOXC1):c.532G>C (p.Asp178His) rs751970827
NM_001453.3(FOXC1):c.807C>G (p.Ser269Arg) rs1277775861

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