List of variants in gene ADGRV1 reported as likely 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: 18

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HGVS	dbSNP	gnomAD frequency
NM_032119.4(ADGRV1):c.327C>T (p.Asp109=)	rs61753944	0.02377
NM_032119.4(ADGRV1):c.8876G>A (p.Arg2959Gln)	rs73175207	0.02358
NM_032119.4(ADGRV1):c.581C>A (p.Pro194His)	rs61745498	0.02028
NM_032119.4(ADGRV1):c.7293C>T (p.Ala2431=)	rs77791584	0.01133
NM_032119.4(ADGRV1):c.1817A>C (p.Asn606Thr)	rs61749567	0.00937
NM_032119.4(ADGRV1):c.3482C>G (p.Ser1161Cys)	rs147062294	0.00492
NM_032119.4(ADGRV1):c.5525-7C>T	rs137853919	0.00429
NM_032119.4(ADGRV1):c.4254T>C (p.Tyr1418=)	rs149459739	0.00414
NM_032119.4(ADGRV1):c.6318G>A (p.Ala2106=)	rs190981860	0.00381
NM_032119.4(ADGRV1):c.8133C>T (p.Ser2711=)	rs116446814	0.00299
NM_032119.4(ADGRV1):c.16472G>A (p.Ser5491Asn)	rs199796758	0.00113
NM_032119.4(ADGRV1):c.16841C>T (p.Thr5614Ile)	rs149544995	0.00082
NM_032119.4(ADGRV1):c.6086C>T (p.Pro2029Leu)	rs200854813	0.00074
NM_032119.4(ADGRV1):c.2241-10A>T	rs150996234	0.00047
NM_032119.4(ADGRV1):c.208-4A>G	rs374070113	0.00034
NM_032119.4(ADGRV1):c.2734+18T>G	rs372642748	0.00022
NM_032119.4(ADGRV1):c.8064C>T (p.Ser2688=)	rs75195840	0.00013
NM_032119.4(ADGRV1):c.11115A>T (p.Ser3705=)	rs138029547

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