List of variants in gene RPS17 studied 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
		ClinVar version:

Total variants: 8

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HGVS	dbSNP	gnomAD frequency
NM_001021.6(RPS17):c.312A>G (p.Glu104=)	rs1049218128	0.02409
NM_001021.6(RPS17):c.328-7G>A	rs975130647	0.00215
GRCh37/hg19 15q25.2(chr15:82631657-83198302)x1
NM_001021.6(RPS17):c.14G>T (p.Arg5Leu)	rs2548306458
NM_001021.6(RPS17):c.152_154del (p.Ala51del)	rs1555451156
NM_001021.6(RPS17):c.159_160delinsCC (p.Val54Leu)
NM_001021.6(RPS17):c.1A>G (p.Met1Val)	rs2548306778
NM_001021.6(RPS17):c.3+132C>G	rs542153649

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