ClinVar Miner

List of variants studied for arthrogryposis by Center for Human Genetics, Inc, Center for Human Genetics, Inc

Included ClinVar conditions (9):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 7
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HGVS dbSNP gnomAD frequency
NM_001999.4(FBN2):c.7471+6G>A rs200998513 0.00205
NM_001999.4(FBN2):c.8282C>T (p.Ala2761Val) rs201962592 0.00021
NM_001999.4(FBN2):c.5303T>C (p.Val1768Ala) rs779202876 0.00001
NM_001999.4(FBN2):c.3459GAA[1] (p.Lys1154del) rs1554123139
NM_001999.4(FBN2):c.3467G>T (p.Cys1156Phe) rs1206843725
NM_001999.4(FBN2):c.3718T>G (p.Cys1240Gly) rs1554122897
NM_001999.4(FBN2):c.4151G>A (p.Cys1384Tyr) rs794727560

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