ClinVar Miner

List of variants reported as benign for congenital vitamin K-dependent coagulation factors deficiency by Illumina Clinical Services Laboratory,Illumina

Included ClinVar conditions (6):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 58
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HGVS dbSNP
NM_000131.4(F7):c.64+9G>A rs6039
NM_000504.4(F10):c.1115G>C (p.Arg372Pro) rs142699098
NM_000504.4(F10):c.111G>A (p.Arg37=) rs115112448
NM_000504.4(F10):c.574G>A (p.Gly192Arg) rs3211783
NM_000504.4(F10):c.792C>T (p.Thr264=) rs5960
NM_000504.4(F10):c.90G>C (p.Gln30His) rs5961
NM_000506.4(F2):c.1233G>A (p.Pro411=) rs5898
NM_000506.4(F2):c.1602G>A (p.Pro534=) rs5900
NM_000506.4(F2):c.1628G>T (p.Arg543Leu) rs143064939
NM_000506.4(F2):c.423-7G>C rs2070852
NM_000506.4(F2):c.480C>T (p.Pro160=) rs3136452
NM_000506.4(F2):c.494C>T (p.Thr165Met) rs5896
NM_000506.4(F2):c.79+7G>A rs3136431
NM_000506.4(F2):c.813C>T (p.Gly271=) rs5899
NM_000506.5(F2):c.*97G>A rs1799963
NM_000506.5(F2):c.843C>T (p.Gly281=) rs147699032
NM_000821.7(GGCX):c.*1049T>A rs13406935
NM_000821.7(GGCX):c.*1727A>T
NM_000821.7(GGCX):c.*1965G>T rs113958713
NM_000821.7(GGCX):c.*225G>A rs72843839
NM_000821.7(GGCX):c.*2381C>T rs6547621
NM_000821.7(GGCX):c.*2949C>T rs76606353
NM_000821.7(GGCX):c.*2974G>A rs72843836
NM_000821.7(GGCX):c.*3047G>A rs34669893
NM_000821.7(GGCX):c.*3053A>G rs150020679
NM_000821.7(GGCX):c.*3071T>C rs72843835
NM_000821.7(GGCX):c.*3398T>C rs35416445
NM_000821.7(GGCX):c.*3416G>A rs6704863
NM_000821.7(GGCX):c.*3431C>T rs72940569
NM_000821.7(GGCX):c.*3606G>A rs535142816
NM_000821.7(GGCX):c.*3752G>A rs72643495
NM_000821.7(GGCX):c.*3805A>G rs12470957
NM_000821.7(GGCX):c.*3875C>T rs58540395
NM_000821.7(GGCX):c.*3996T>C rs12473819
NM_000821.7(GGCX):c.*4429G>A rs62165899
NM_000821.7(GGCX):c.*4509G>A rs7605975
NM_000821.7(GGCX):c.*4579G>A rs138686161
NM_000821.7(GGCX):c.*4840T>C
NM_000821.7(GGCX):c.*902T>C rs6723678
NM_000821.7(GGCX):c.1218C>T (p.Arg406=) rs2592551
NM_000821.7(GGCX):c.1242C>T (p.Thr414=) rs10179904
NM_000821.7(GGCX):c.1494C>T (p.Arg498=) rs41290033
NM_000821.7(GGCX):c.1806C>G (p.Val602=) rs143538795
NM_000821.7(GGCX):c.339C>T (p.Asp113=) rs6751560
NM_000821.7(GGCX):c.91G>A (p.Asp31Asn)
NM_000821.7(GGCX):c.974G>A (p.Arg325Gln) rs699664
NM_019616.4(F7):c.*620C>T rs151109093
NM_019616.4(F7):c.*770G>A rs3093253
NM_019616.4(F7):c.1172G>A (p.Arg391Gln) rs6046
NM_019616.4(F7):c.219G>A (p.Glu73=) rs36208758
NM_019616.4(F7):c.459C>T (p.His153=) rs6042
NM_019616.4(F7):c.483C>T (p.Asp161=) rs6040
NM_019616.4(F7):c.64+941C>T
NM_024006.6(VKORC1):c.*134G>A rs7294
NM_024006.6(VKORC1):c.196G>A (p.Val66Met) rs72547529
NM_024006.6(VKORC1):c.203A>G (p.His68Arg)
NM_024006.6(VKORC1):c.358C>T (p.Leu120=) rs7200749
NM_024006.6(VKORC1):c.36G>A (p.Arg12=) rs55894764

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