List of variants in gene ROBO2 studied for Congenital anomaly of kidney and urinary tract

Minimum submission review status:		Collection method:
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Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 18

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HGVS	dbSNP	gnomAD frequency
NM_001395656.1(ROBO2):c.1556A>T (p.Asn519Ile)	rs80051448	0.00662
NM_001395656.1(ROBO2):c.2443C>T (p.Arg815Trp)	rs188582283	0.00410
NM_001395656.1(ROBO2):c.1930C>T (p.Arg644Cys)	rs763833545	0.00004
NM_001395656.1(ROBO2):c.2402G>A (p.Arg801Gln)	rs201678507	0.00003
NM_001395656.1(ROBO2):c.1576C>A (p.Pro526Thr)	rs750974106	0.00002
NM_001395656.1(ROBO2):c.3718G>A (p.Ala1240Thr)	rs267607015	0.00002
NM_001395656.1(ROBO2):c.2309A>G (p.Asp770Gly)	rs1559650461	0.00001
NM_001395656.1(ROBO2):c.2846T>C (p.Ile949Thr)	rs267607014	0.00001
NM_001395656.1(ROBO2):c.3724G>A (p.Asp1242Asn)	rs1333751060	0.00001
NM_001395656.1(ROBO2):c.2275A>C (p.Ser759Arg)	rs910956713
NM_001395656.1(ROBO2):c.2407G>A (p.Val803Ile)	rs759802937
NM_001395656.1(ROBO2):c.292G>T (p.Gly98Trp)	rs2071367863
NM_001395656.1(ROBO2):c.335C>T (p.Ala112Val)	rs780623744
NM_001395656.1(ROBO2):c.3830_3832del (p.Ser1277del)	rs2095237973
NM_001395656.1(ROBO2):c.676A>G (p.Thr226Ala)	rs2086360838
NM_001395656.1(ROBO2):c.760C>G (p.Pro254Ala)	rs772503893
NM_001395656.1(ROBO2):c.95G>A (p.Arg32Gln)	rs754279676
NM_001395656.1(ROBO2):c.994G>A (p.Gly332Ser)	rs986191822

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