List of variants in gene RPS19 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: 14

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HGVS	dbSNP	gnomAD frequency
NM_001022.4(RPS19):c.60C>G (p.Ala20=)	rs149249194	0.00108
NM_001022.4(RPS19):c.1-14A>G	rs201317022	0.00044
NM_001022.4(RPS19):c.164C>T (p.Thr55Met)	rs147508369	0.00039
NM_001022.4(RPS19):c.1-13C>T	rs200634600	0.00028
NM_001022.4(RPS19):c.333A>G (p.Lys111=)	rs781845960	0.00008
NM_001022.4(RPS19):c.183G>A (p.Ala61=)	rs782727047	0.00006
NM_001022.4(RPS19):c.208G>A (p.Ala70Thr)	rs782368794	0.00006
NM_001022.4(RPS19):c.411+19G>T	rs782394063	0.00006
NM_001022.4(RPS19):c.72-17C>G	rs150151184	0.00004
NM_001022.4(RPS19):c.128A>G (p.Lys43Arg)	rs1400674746	0.00001
NM_001022.4(RPS19):c.356+12del	rs781789110	0.00001
NM_001022.4(RPS19):c.245G>A (p.Arg82His)	rs782814286
NM_001022.4(RPS19):c.356+18G>C	rs61762294
NM_001022.4(RPS19):c.75C>T (p.Ser25=)	rs370343297

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