ClinVar Miner

List of variants reported as benign for congenital factor X deficiency by Illumina Laboratory Services, Illumina

Included ClinVar conditions (3):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 7
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HGVS dbSNP gnomAD frequency
NM_000504.4(F10):c.792C>T (p.Thr264=) rs5960 0.72493
NM_019616.4(F7):c.1172G>A (p.Arg391Gln) rs6046 0.11103
NM_019616.4(F7):c.*770G>A rs3093253 0.10963
NM_000504.4(F10):c.574G>A (p.Gly192Arg) rs3211783 0.02730
NM_000504.4(F10):c.90G>C (p.Gln30His) rs5961 0.01285
NM_000504.4(F10):c.111G>A (p.Arg37=) rs115112448 0.00649
NM_000504.4(F10):c.1115G>C (p.Arg372Pro) rs142699098

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