List of variants in gene RMRP reported as uncertain significance by Fulgent Genetics, Fulgent Genetics

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: 25

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HGVS	dbSNP	gnomAD frequency
NR_003051.4(RMRP):n.125C>A	rs758130879	0.00022
NR_003051.4(RMRP):n.2G>A	rs773520232	0.00019
NC_000009.12:g.35657748A>G	rs377349293	0.00007
NR_003051.4(RMRP):n.194C>T	rs1045976155	0.00006
NR_003051.4(RMRP):n.137C>T	rs940224067	0.00005
NR_003051.4(RMRP):n.36A>G	rs572081363	0.00005
NC_000009.12:g.35658039T>G	rs563106486	0.00003
NC_000009.12:g.35658044T>C	rs1479868789	0.00003
NR_003051.4(RMRP):n.134C>T	rs1587918293	0.00001
NR_003051.4(RMRP):n.202C>T	rs1245933575	0.00001
NR_003051.4(RMRP):n.97G>A	rs970510851	0.00001
NC_000009.12:g.35658020C>A	rs958637129
NC_000009.12:g.35658027A>G	rs12552387
NC_000009.12:g.35658036G>A	rs775303012
NC_000009.12:g.35658038G>A	rs183974004
NC_000009.12:g.35658042T>G	rs529852688
NC_000009.12:g.35658049T>C	rs145463993
NR_003051.3(RMRP):n.-12dup	rs1554651504
NR_003051.3(RMRP):n.-21_-19dup	rs1029136594
NR_003051.4(RMRP):n.115C>T	rs769331218
NR_003051.4(RMRP):n.125_126dup	rs1554651193
NR_003051.4(RMRP):n.147C>A	rs757576534
NR_003051.4(RMRP):n.154A>G	rs1428585182
NR_003051.4(RMRP):n.242A>C	rs1038523315
NR_003051.4(RMRP):n.87C>G	rs545284014

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