List of variants studied for Marshall syndrome by Illumina Laboratory Services, Illumina

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
		ClinVar version:

Total variants: 15

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HGVS	dbSNP	gnomAD frequency
NM_001854.4(COL11A1):c.*628dup	rs532806397	0.00093
NM_001854.4(COL11A1):c.-198_-195del	rs886044981	0.00031
NM_001854.4(COL11A1):c.4140+13del	rs781736900	0.00012
NM_001854.4(COL11A1):c.-231dup	rs886044983
NM_001854.4(COL11A1):c.1792-39ATG[11]	rs71752747
NM_001854.4(COL11A1):c.1792-39ATG[12]	rs71752747
NM_001854.4(COL11A1):c.1792-39ATG[8]	rs71752747
NM_001854.4(COL11A1):c.3817-13del	rs34228277
NM_001854.4(COL11A1):c.3817-14_3817-13dup	rs34228277
NM_001854.4(COL11A1):c.4303-13del	rs35232764
NM_001854.4(COL11A1):c.4303-13dup	rs35232764
NM_001854.4(COL11A1):c.4357-16dup	rs748850423
NM_001854.4(COL11A1):c.652-6dup	rs36076089
NM_001854.4(COL11A1):c.652-7_652-6del	rs36076089
NM_001854.4(COL11A1):c.652-7_652-6dup	rs36076089

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