List of variants reported as benign for Griscelli syndrome type 2 by Illumina Laboratory Services, Illumina

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Total variants: 23

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HGVS	dbSNP	gnomAD frequency
NM_183235.3(RAB27A):c.*1926T>A	rs8028801	0.33811
NM_183235.3(RAB27A):c.*852C>T	rs3179664	0.33294
NM_183235.3(RAB27A):c.*1931T>C	rs6493770	0.27860
NM_183235.3(RAB27A):c.*14C>T	rs1050931	0.27464
NM_183235.3(RAB27A):c.*1662A>T	rs1061823	0.27450
NM_183235.3(RAB27A):c.*936C>A	rs1061870	0.27449
NM_183235.3(RAB27A):c.*949A>G	rs1061873	0.27447
NM_183235.3(RAB27A):c.*1594A>G	rs1061821	0.27431
NM_183235.3(RAB27A):c.*1647T>G	rs1061822	0.27431
NM_183235.3(RAB27A):c.*1742A>G	rs1061824	0.27430
NM_183235.3(RAB27A):c.*1427G>A	rs1061875	0.27307
NM_183235.3(RAB27A):c.*1418T>A	rs1061874	0.27298
NM_183235.3(RAB27A):c.*2007G>A	rs6493769	0.27179
NM_183235.3(RAB27A):c.*1392A>C	rs12907749	0.11078
NM_183235.3(RAB27A):c.*2067C>G	rs7168226	0.10411
NM_183235.3(RAB27A):c.*731G>T	rs76097718	0.02129
NM_183235.3(RAB27A):c.-142-5A>G	rs61436564	0.01642
NM_183235.3(RAB27A):c.*842G>A	rs59982153	0.01444
NM_183235.3(RAB27A):c.*2349A>G	rs76970799	0.01147
NM_183235.3(RAB27A):c.*387A>G	rs73407873	0.00697
NM_183235.3(RAB27A):c.*472A>C	rs116723038	0.00475
NM_183235.3(RAB27A):c.*1013T>C	rs190724892	0.00420
NM_183235.3(RAB27A):c.594G>A (p.Val198=)	rs141222527	0.00374

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