List of variants in gene RPS7 reported as benign for not provided

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

Total variants: 20

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HGVS	dbSNP	gnomAD frequency
NM_001011.4(RPS7):c.357-52G>C	rs7576238	0.83566
NM_001011.4(RPS7):c.147+62A>G	rs3087873	0.77182
NM_001011.4(RPS7):c.292-233T>C	rs9808074	0.21982
NM_001011.4(RPS7):c.292-121C>T	rs72767177	0.21593
NM_001011.4(RPS7):c.508-12C>A	rs2071639	0.12923
NM_001011.4(RPS7):c.292-262G>T	rs75452965	0.09045
NM_001011.4(RPS7):c.148-194C>T	rs62106032	0.06747
NM_001011.4(RPS7):c.291+83G>A	rs80103345	0.05422
NM_001011.4(RPS7):c.292-153G>C	rs62106037	0.05419
NM_001011.4(RPS7):c.-47G>T	rs11558965	0.05356
NM_001011.4(RPS7):c.148-138T>C	rs62106033	0.05249
NM_001011.4(RPS7):c.356+65A>G	rs73137100	0.04530
NM_001011.4(RPS7):c.508-197C>T	rs59060135	0.04202
NM_001011.4(RPS7):c.147+77G>C	rs59077127	0.04057
NM_001011.4(RPS7):c.292-39C>T	rs73910594	0.03067
NM_001011.4(RPS7):c.147+63G>A	rs11683831	0.01796
NC_000002.12:g.3575072G>T	rs115090628	0.00123
NM_001011.4(RPS7):c.148-26C>A	rs62106034
NM_001011.4(RPS7):c.292-125T>C	rs72767176
NM_001011.4(RPS7):c.357-3dup	rs140914434

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