ClinVar Miner

List of variants in gene ADCK2, AGBL3, AGK, AKR1B1, AKR1B10, AKR1B15, AKR1D1, ARHGEF35, ARHGEF5, ATP6V0A4, BPGM, BRAF, CALD1, CASP2, CHRM2, CLCN1, CLEC2L, CLEC5A, CNOT4, CNTNAP2, CREB3L2, CTAGE15, CTAGE4, CTAGE6, CTAGE8, CYREN, DENND11, DENND2A, DGKI, EPHA1, EPHB6, FAM131B, FAM180A, FMC1, FMC1-LUC7L2, GSTK1, IFT56, KDM7A, KEL, KIAA1549, KLRG2, LLCFC1, LRGUK, LUC7L2, LUZP6, MGAM, MKRN1, MRPS33, MTPN, MTRNR2L6, NDUFB2, NOBOX, NUP205, OR2A1, OR2A12, OR2A14, OR2A2, OR2A25, OR2A42, OR2A5, OR2A7, OR2F1, OR2F2, OR6B1, OR6V1, OR9A2, OR9A4, PARP12, PIP, PRSS1, PRSS37, PRSS58, PTN, RAB19, SLC13A4, SLC35B4, SLC37A3, SSBP1, STMP1, STRA8, SVOPL, TAS2R3, TAS2R38, TAS2R39, TAS2R4, TAS2R40, TAS2R41, TAS2R5, TAS2R60, TBXAS1, TCAF1, TCAF2, TMEM139, TMEM140, TMEM178B, TMEM213, TPK1, TRB, TRIM24, TRPV5, TRPV6, UBN2, WDR91, WEE2, ZC3HAV1, ZC3HAV1L, ZYX studied for Hypertelorism; Global developmental delay; Growth delay; Abnormal facial shape; Small face; Wide mouth; Floppy infant; Short finger

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
GRCh37/hg19 7q33-35(chr7:133848099-145814115)x1

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