List of variants in gene combination FANCL, VRK2 reported as uncertain significance for immune system disorder

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: 21

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HGVS	dbSNP	gnomAD frequency
NM_006296.7(VRK2):c.1303G>A (p.Asp435Asn)	rs201610023	0.00004
NM_018062.4(FANCL):c.*515A>C	rs971589098	0.00003
NM_018062.4(FANCL):c.1121A>G (p.Lys374Arg)	rs745544496	0.00003
NC_000002.11:g.(?_58386900)_(58390229_?)dup
NC_000002.11:g.(?_58386900)_(58393029_?)dup
NC_000002.11:g.(?_58386900)_(58459257_?)dup
NC_000002.11:g.(?_58386900)_(58468448_?)dup
NC_000002.12:g.(?_58159755)_(58241323_?)dup
NM_006296.7(VRK2):c.102_105dup	rs759217526
NM_018062.4(FANCL):c.*128G>A	rs781556579
NM_018062.4(FANCL):c.*165A>C	rs866675905
NM_018062.4(FANCL):c.*165A>G	rs866675905
NM_018062.4(FANCL):c.*281C>G	rs951671744
NM_018062.4(FANCL):c.*434A>G	rs1395685917
NM_018062.4(FANCL):c.447_450del	rs748896681
NM_018062.4(FANCL):c.*89C>T	rs1684780470
NM_018062.4(FANCL):c.1093-13T>A
NM_018062.4(FANCL):c.1096A>G (p.Ile366Val)
NM_018062.4(FANCL):c.1109T>C (p.Met370Thr)	rs1684813547
NM_018062.4(FANCL):c.1118G>C (p.Arg373Thr)
NM_018062.4(FANCL):c.1123C>G (p.His375Asp)

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