List of variants in gene RPS19 reported as benign for hematologic disorder

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

Total variants: 17

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HGVS	dbSNP	gnomAD frequency
NM_001022.4(RPS19):c.356+14=	rs1366610	0.99999
NM_001022.4(RPS19):c.411+12G>A	rs61762296	0.00287
NM_001022.3(RPS19):c.-234G>A	rs142324259	0.00161
NM_001022.4(RPS19):c.60C>G (p.Ala20=)	rs149249194	0.00108
NM_001022.3(RPS19):c.-274T>C	rs77406992	0.00036
NM_001022.4(RPS19):c.68A>G (p.Lys23Arg)	rs143477104	0.00029
NM_001022.4(RPS19):c.1-13C>T	rs200634600	0.00028
NM_001022.3(RPS19):c.-288A>C	rs192556926	0.00024
NM_001022.4(RPS19):c.173-19C>G	rs782495262	0.00006
NM_001022.4(RPS19):c.72-17C>G	rs150151184	0.00004
NM_001022.4(RPS19):c.411+6G>C	rs138397598	0.00003
NM_001022.3(RPS19):c.-146_-145insGCCA	rs34020014
NM_001022.4(RPS19):c.-1+26G>T	rs74449035
NM_001022.4(RPS19):c.356+14delinsGG
NM_001022.4(RPS19):c.356+169CT[2]	rs369353222
NM_001022.4(RPS19):c.356+18G>C	rs61762294
NM_001022.4(RPS19):c.71+12del	rs886054470

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