List of variants in gene RMRP reported as uncertain significance by Women's Health and Genetics/Laboratory Corporation of America, LabCorp

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: 24

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HGVS	dbSNP	gnomAD frequency
NR_003051.3(RMRP):n.-12A>C	rs372044910	0.00058
NR_003051.4(RMRP):n.59_60insA	rs1053360711	0.00021
NR_003051.3(RMRP):n.-22T>C	rs947939533	0.00008
NR_003051.3(RMRP):n.271T>C	rs377349293	0.00007
NR_003051.4(RMRP):n.16G>T	rs902313238	0.00002
NC_000009.12:g.35658023_35658024delinsTT	rs2131809702
NR_003051.3(RMRP):n.-20C>T	rs183974004
NR_003051.3(RMRP):n.-6G>C	rs191438045
NR_003051.3(RMRP):n.157_159delinsCTG
NR_003051.4(RMRP):n.107C>G
NR_003051.4(RMRP):n.11T>C	rs748814304
NR_003051.4(RMRP):n.144G>A	rs113967059
NR_003051.4(RMRP):n.184G>A	rs1554651153
NR_003051.4(RMRP):n.19_20insA
NR_003051.4(RMRP):n.216A>G	rs886041234
NR_003051.4(RMRP):n.217G>A
NR_003051.4(RMRP):n.219C>T
NR_003051.4(RMRP):n.242A>C	rs1038523315
NR_003051.4(RMRP):n.254T>G
NR_003051.4(RMRP):n.262G>A	rs769080777
NR_003051.4(RMRP):n.52C>T	rs1064793373
NR_003051.4(RMRP):n.63G>A	rs544069410
NR_003051.4(RMRP):n.63G>C	rs544069410
NR_003051.4(RMRP):n.87C>T	rs545284014

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