ClinVar Miner

List of variants reported as uncertain significance for Factor XII deficiency disease by Illumina Laboratory Services, Illumina

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Total variants: 26
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HGVS dbSNP gnomAD frequency
NM_000505.4(F12):c.1018+13G>C rs552424629 0.00239
NM_000505.4(F12):c.1018+12G>C rs758462343 0.00082
NM_000505.4(F12):c.348C>A (p.Gly116=) rs140243617 0.00081
NM_000505.4(F12):c.120C>T (p.Leu40=) rs149368999 0.00073
NM_000505.4(F12):c.1107G>C (p.Ser369=) rs141473119 0.00063
NM_000505.4(F12):c.1387+4C>G rs761161412 0.00014
NM_000505.4(F12):c.-3G>A rs201346142 0.00011
NM_000505.4(F12):c.1212C>G (p.Pro404=) rs756802257 0.00005
NM_000505.4(F12):c.129C>T (p.Thr43=) rs201546796 0.00004
NM_000505.4(F12):c.1018+14G>T rs779057710 0.00003
NM_000505.4(F12):c.1251-12C>A rs747726864 0.00003
NM_000505.4(F12):c.1704G>A (p.Val568=) rs536390950 0.00003
NM_000505.4(F12):c.630C>T (p.Asp210=) rs886060471 0.00003
NM_000505.4(F12):c.928A>T (p.Arg310Trp) rs749549919 0.00003
NM_000505.4(F12):c.*86C>T rs777897437 0.00001
NM_000505.4(F12):c.*9G>A rs1763150862 0.00001
NM_000505.4(F12):c.158A>G (p.Tyr53Cys) rs118204455 0.00001
NM_000505.4(F12):c.293G>A (p.Cys98Tyr) rs770412757 0.00001
NM_000505.4(F12):c.30G>A (p.Leu10=) rs745617919 0.00001
NM_000505.4(F12):c.-25G>A rs886060472
NM_000505.4(F12):c.1018+11G>T rs570973405
NM_000505.4(F12):c.1025C>T (p.Pro342Leu) rs2230939
NM_000505.4(F12):c.1142G>A (p.Arg381His) rs1763214147
NM_000505.4(F12):c.1251-9C>A rs17876032
NM_000505.4(F12):c.286+6A>G rs1763273226
NM_000505.4(F12):c.957G>C (p.Gln319His) rs1763225226

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