List of variants in gene GGCX reported as benign for congenital vitamin K-dependent coagulation factors deficiency

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 29

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HGVS	dbSNP	gnomAD frequency
NM_000821.7(GGCX):c.*3996T>C	rs12473819	0.55548
NM_000821.7(GGCX):c.*2381C>T	rs6547621	0.52266
NM_000821.7(GGCX):c.*4509G>A	rs7605975	0.52251
NM_000821.7(GGCX):c.974G>A (p.Arg325Gln)	rs699664	0.41038
NM_000821.7(GGCX):c.1218C>T (p.Arg406=)	rs2592551	0.30130
NM_000821.7(GGCX):c.*3398T>C	rs35416445	0.30037
NM_000821.7(GGCX):c.*3805A>G	rs12470957	0.12606
NM_000821.7(GGCX):c.*3752G>A	rs72643495	0.12184
NM_000821.7(GGCX):c.*1049T>A	rs13406935	0.11064
NM_000821.7(GGCX):c.*4429G>A	rs62165899	0.11060
NM_000821.7(GGCX):c.1242C>T (p.Thr414=)	rs10179904	0.11053
NM_000821.7(GGCX):c.*3047G>A	rs34669893	0.10244
NM_000821.7(GGCX):c.*3416G>A	rs6704863	0.08578
NM_000821.7(GGCX):c.*3071T>C	rs72843835	0.07788
NM_000821.7(GGCX):c.*2974G>A	rs72843836	0.07770
NM_000821.7(GGCX):c.*225G>A	rs72843839	0.06084
NM_000821.7(GGCX):c.339C>T (p.Asp113=)	rs6751560	0.04827
NM_000821.7(GGCX):c.*2949C>T	rs76606353	0.03766
NM_000821.7(GGCX):c.*3875C>T	rs58540395	0.02955
NM_000821.7(GGCX):c.*902T>C	rs6723678	0.02953
NM_000821.7(GGCX):c.*1965G>T	rs113958713	0.02948
NM_000821.7(GGCX):c.*3431C>T	rs72940569	0.02772
NM_000821.7(GGCX):c.*4579G>A	rs138686161	0.01846
NM_000821.7(GGCX):c.1494C>T (p.Arg498=)	rs41290033	0.01507
NM_000821.7(GGCX):c.*3053A>G	rs150020679	0.00896
NM_000821.7(GGCX):c.1806C>G (p.Val602=)	rs143538795	0.00758
NM_000821.7(GGCX):c.91G>A (p.Asp31Asn)	rs74843621	0.00126
NM_000821.7(GGCX):c.*3606G>A	rs535142816	0.00004
NM_000821.7(GGCX):c.*1727A>T	rs114386392

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