List of variants in gene SMARCA2 reported by Baylor 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: 16

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HGVS	dbSNP	gnomAD frequency
NM_003070.5(SMARCA2):c.2564G>A (p.Arg855Gln)	rs1471482709	0.00001
NM_003070.5(SMARCA2):c.4765G>C (p.Asp1589His)	rs1380500654	0.00001
NM_003070.5(SMARCA2):c.-37+1G>T
NM_003070.5(SMARCA2):c.2254G>A (p.Gly752Arg)	rs1821581008
NM_003070.5(SMARCA2):c.2267C>T (p.Thr756Ile)	rs281875191
NM_003070.5(SMARCA2):c.2348C>T (p.Ser783Leu)	rs1554623112
NM_003070.5(SMARCA2):c.2361C>A (p.Asn787Lys)	rs1343138502
NM_003070.5(SMARCA2):c.2554G>C (p.Glu852Gln)	rs281875199
NM_003070.5(SMARCA2):c.2648C>T (p.Pro883Leu)	rs281875188
NM_003070.5(SMARCA2):c.274G>A (p.Gly92Arg)	rs1316406047
NM_003070.5(SMARCA2):c.2810G>A (p.Arg937His)	rs1586692551
NM_003070.5(SMARCA2):c.3314G>A (p.Arg1105His)	rs281875197
NM_003070.5(SMARCA2):c.3448C>G (p.Pro1150Ala)	rs1822944896
NM_003070.5(SMARCA2):c.3476G>A (p.Arg1159Gln)	rs281875187
NM_003070.5(SMARCA2):c.4696G>A (p.Val1566Ile)	rs1827870545
NM_003070.5(SMARCA2):c.4708T>C (p.Phe1570Leu)	rs1373182486

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