ClinVar Miner

List of variants studied for EIG by Fulgent Genetics,Fulgent Genetics

Included ClinVar conditions (4):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 5
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HGVS dbSNP
NM_001082575.2(RBFOX3):c.19C>T (p.Pro7Ser) rs376060745
NM_001082575.2(RBFOX3):c.347G>A (p.Arg116Gln) rs199891032
NM_018723.4(RBFOX1):c.1033G>A (p.Ala345Thr) rs150941982
NM_018723.4(RBFOX1):c.293C>T (p.Thr98Met) rs373077021
NM_018723.4(RBFOX1):c.52C>G (p.Pro18Ala) rs149974858

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