List of variants in gene RPS7 reported by Illumina Laboratory Services, Illumina

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: 17

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HGVS	dbSNP	gnomAD frequency
NM_001011.4(RPS7):c.508-12C>A	rs2071639	0.12923
NM_001011.4(RPS7):c.-47G>T	rs11558965	0.05356
NM_001011.4(RPS7):c.-36A>C	rs17552296	0.00303
NM_001011.4(RPS7):c.-104G>A	rs371620447	0.00022
NM_001011.4(RPS7):c.*31C>T	rs191506876	0.00021
NM_001011.4(RPS7):c.435C>T (p.Arg145=)	rs142207795	0.00009
NM_001011.4(RPS7):c.-27C>T	rs573443780	0.00006
NM_001011.4(RPS7):c.75+13C>T	rs751796318	0.00006
NM_001011.4(RPS7):c.-86C>T	rs186304514	0.00003
NM_001011.4(RPS7):c.-23G>A	rs886055985	0.00002
NM_001011.4(RPS7):c.-44C>T	rs563293592	0.00002
NM_001011.4(RPS7):c.-13C>T	rs765604580	0.00001
NM_001011.4(RPS7):c.39C>T (p.Gly13=)	rs746686516	0.00001
NM_001011.4(RPS7):c.-109C>T	rs142444366
NM_001011.4(RPS7):c.-19+13C>T	rs530845583
NM_001011.4(RPS7):c.292-9A>T	rs746941533
NM_001011.4(RPS7):c.580T>C (p.Leu194=)	rs1480952113

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