ClinVar Miner

List of variants in gene B4GALT7, DBN1, DDX41, DOK3, F12, FAM193B, GRK6, LMAN2, MXD3, NSD1, PDLIM7, PFN3, PRELID1, PRR7, RAB24, RGS14, SLC34A1, TMED9 studied for syndrome caused by partial chromosomal deletion

Included ClinVar conditions (110):

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 1

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HGVS	dbSNP	gnomAD frequency
NC_000005.9:g.(?_176618865)_(177036696_?)dup

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