ClinVar Miner

List of variants reported as likely benign for Fanconi anemia complementation group G by Illumina Laboratory Services, Illumina

Included ClinVar conditions (1):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 6
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HGVS dbSNP gnomAD frequency
NM_004629.2(FANCG):c.1133C>T (p.Ser378Leu) rs4986939 0.03269
NM_004629.2(FANCG):c.238C>T (p.Leu80=) rs115131067 0.00330
NM_004629.1(FANCG):c.-450G>C rs535301610 0.00283
NM_004629.2(FANCG):c.1638T>C (p.Gly546=) rs45537335 0.00175
NM_004629.2(FANCG):c.-93C>G rs532840867 0.00004
NM_004629.2(FANCG):c.-342G>T rs556082635

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