List of variants in gene GCM2 reported 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
		ClinVar version:

Total variants: 15

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HGVS	dbSNP	gnomAD frequency
NM_004752.4(GCM2):c.1060A>G (p.Met354Val)	rs61734278	0.01292
NM_004752.4(GCM2):c.943A>G (p.Asn315Asp)	rs114070356	0.00258
NM_004752.4(GCM2):c.306G>A (p.Arg102=)	rs149143032	0.00142
NM_004752.4(GCM2):c.1181A>C (p.Tyr394Ser)	rs142287570	0.00050
NM_004752.4(GCM2):c.319G>A (p.Asp107Asn)	rs61741855	0.00043
NM_004752.4(GCM2):c.1063G>A (p.Ala355Thr)	rs764488668	0.00007
NM_004752.4(GCM2):c.1144G>A (p.Val382Met)	rs371918069	0.00006
NM_004752.4(GCM2):c.1364G>A (p.Arg455Gln)	rs145103332	0.00004
NM_004752.4(GCM2):c.318C>T (p.Cys106=)	rs749600723	0.00004
NM_004752.4(GCM2):c.187G>A (p.Gly63Ser)	rs104893960	0.00003
NM_004752.4(GCM2):c.116G>A (p.Arg39Gln)	rs534895356	0.00001
NM_004752.4(GCM2):c.1504A>C (p.Asn502His)	rs533942394	0.00001
NM_004752.4(GCM2):c.1177_1185dup (p.Ala393_Gln395dup)	rs551375300
NM_004752.4(GCM2):c.129C>G (p.Asp43Glu)	rs141188465
NM_004752.4(GCM2):c.307C>T (p.Pro103Ser)	rs1561672362

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