List of variants in gene ADGRV1 reported as benign by Fulgent Genetics, Fulgent Genetics

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 14

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HGVS	dbSNP	gnomAD frequency
NM_032119.4(ADGRV1):c.6695A>G (p.Tyr2232Cys)	rs10037067	0.33642
NM_032119.4(ADGRV1):c.5960C>T (p.Pro1987Leu)	rs4916685	0.32486
NM_032119.4(ADGRV1):c.7206G>A (p.Glu2402=)	rs16876822	0.31193
NM_032119.4(ADGRV1):c.7034A>G (p.Asn2345Ser)	rs2366926	0.31179
NM_032119.4(ADGRV1):c.6952-10G>A	rs10040165	0.31172
NM_032119.4(ADGRV1):c.9927T>G (p.Pro3309=)	rs16869042	0.30112
NM_032119.4(ADGRV1):c.13599A>G (p.Thr4533=)	rs17554631	0.15645
NM_032119.4(ADGRV1):c.18741G>A (p.Gly6247=)	rs13158963	0.11513
NM_032119.4(ADGRV1):c.8730+10_8730+11insC	rs377585302	0.06843
NM_032119.4(ADGRV1):c.4506C>T (p.Pro1502=)	rs17543819	0.05741
NM_032119.4(ADGRV1):c.7229A>G (p.Tyr2410Cys)	rs111033430	0.02235
NM_032119.4(ADGRV1):c.1652T>C (p.Val551Ala)	rs6889939	0.01679
NM_032119.4(ADGRV1):c.7079G>A (p.Arg2360His)	rs111033470	0.00784
NM_032119.4(ADGRV1):c.13037C>T (p.Pro4346Leu)	rs74632023	0.00712

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