List of variants in gene RMRP 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: 36

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HGVS	dbSNP	gnomAD frequency
NR_003051.4(RMRP):n.158G>C	rs7021463	0.17549
NR_003051.4(RMRP):n.129G>C	rs74810894	0.00319
NR_003051.4(RMRP):n.55C>T	rs193117694	0.00303
NR_003051.3(RMRP):n.-12A>C	rs372044910	0.00058
NR_003051.4(RMRP):n.141A>G	rs578091934	0.00042
NR_003051.4(RMRP):n.6C>T	rs772443941	0.00016
NC_000009.12:g.35657746A>G	rs749839597	0.00009
NR_003051.3(RMRP):n.-19_-13dup	rs1554651506	0.00005
NR_003051.3(RMRP):n.64C>T	rs786204684	0.00004
NR_003051.4(RMRP):n.81G>A	rs756128568	0.00004
NR_003051.4(RMRP):n.16G>T	rs902313238	0.00002
NR_003051.4(RMRP):n.192T>G	rs1303560278	0.00001
NR_003051.4(RMRP):n.7G>A	rs552002151	0.00001
NC_000009.12:g.35658022_35658032dup	rs1554651425
NC_000009.12:g.35658023_35658038dup	rs1823637651
NR_003051.3(RMRP):n.-19_-3dup	rs727502778
NR_003051.3(RMRP):n.-20C>G	rs183974004
NR_003051.3(RMRP):n.-24_-10dup	rs727502776
NR_003051.3(RMRP):n.-25_-7dup	rs1554651455
NR_003051.3(RMRP):n.-53A>G	rs551474332
NR_003051.3(RMRP):n.-5G>A	rs7024732
NR_003051.3(RMRP):n.-9T>G	rs12552387
NR_003051.3(RMRP):n.146C>T	rs757576534
NR_003051.3(RMRP):n.147G>A	rs753874439
NR_003051.4(RMRP):n.149C>T	rs1085307765
NR_003051.4(RMRP):n.154A>G	rs1428585182
NR_003051.4(RMRP):n.197C>T	rs948931144
NR_003051.4(RMRP):n.1T>C	rs188190570
NR_003051.4(RMRP):n.216A>C	rs886041234
NR_003051.4(RMRP):n.264G>C	rs727502774
NR_003051.4(RMRP):n.267T>C	rs557906740
NR_003051.4(RMRP):n.47T>A	rs529328233
NR_003051.4(RMRP):n.52C>T	rs1064793373
NR_003051.4(RMRP):n.94A>G	rs928762713
NR_003051.4(RMRP):n.97_98dup	rs1340624774
NR_003051.4(RMRP):n.99G>A	rs915919453

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