ClinVar Miner

List of variants in gene RMRP studied for not specified

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 68
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HGVS dbSNP gnomAD frequency
NC_000009.12:g.35658065G>T rs3829076 0.46029
NR_003051.4(RMRP):n.179C>T rs7021642 0.17814
NR_003051.4(RMRP):n.158G>C rs7021463 0.17549
NR_003051.4(RMRP):n.129G>C rs74810894 0.00319
NC_000009.12:g.35658021G>A rs138660393 0.00185
NC_000009.12:g.35658030T>G rs372044910 0.00058
NC_000009.12:g.35658025T>C rs111909453 0.00057
NR_003051.4(RMRP):n.141A>G rs578091934 0.00042
NR_003051.4(RMRP):n.177G>A rs377566038 0.00039
NR_003051.4(RMRP):n.125C>A rs758130879 0.00022
NR_003051.4(RMRP):n.59_60insA rs1053360711 0.00021
NR_003051.4(RMRP):n.2G>A rs773520232 0.00019
NR_003051.4(RMRP):n.181dup rs940080676 0.00015
NC_000009.12:g.35657746A>G rs749839597 0.00009
NC_000009.12:g.35658040A>G rs947939533 0.00008
NC_000009.12:g.35657748A>G rs377349293 0.00007
NR_003051.4(RMRP):n.194C>T rs1045976155 0.00003
NR_003051.4(RMRP):n.16G>T rs902313238 0.00002
NR_003051.4(RMRP):n.265G>A rs578123788 0.00002
NR_003051.4(RMRP):n.86T>G rs991322091 0.00001
NC_000009.12:g.35657747A>G
NC_000009.12:g.35657873G>A rs757576534
NC_000009.12:g.35658022T>C rs555890962
NC_000009.12:g.35658023C>G rs7024732
NC_000009.12:g.35658023_35658024delinsTT rs2131809702
NC_000009.12:g.35658024C>G rs191438045
NC_000009.12:g.35658027A>C rs12552387
NC_000009.12:g.35658027A>G rs12552387
NC_000009.12:g.35658038G>A rs183974004
NC_000009.12:g.35658038G>C rs183974004
NC_000009.12:g.35658041G>C rs188660894
NC_000009.12:g.35658045T>C
NC_000009.12:g.35658074G>C rs531089786
NC_000009.12:g.35658122G>A rs1554651647
NR_003051.4(RMRP):n.101C>G rs536333075
NR_003051.4(RMRP):n.101C>T rs536333075
NR_003051.4(RMRP):n.107C>G
NR_003051.4(RMRP):n.11T>C rs748814304
NR_003051.4(RMRP):n.126C>T
NR_003051.4(RMRP):n.13A>G
NR_003051.4(RMRP):n.144G>A rs113967059
NR_003051.4(RMRP):n.149C>G
NR_003051.4(RMRP):n.158_160delinsCTG
NR_003051.4(RMRP):n.184G>A rs1554651153
NR_003051.4(RMRP):n.195G>C rs761398394
NR_003051.4(RMRP):n.195G>T
NR_003051.4(RMRP):n.19_20insA
NR_003051.4(RMRP):n.205T>G
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.244A>C rs551450545
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.54dup rs151011853
NR_003051.4(RMRP):n.63G>A rs544069410
NR_003051.4(RMRP):n.63G>C rs544069410
NR_003051.4(RMRP):n.65C>A
NR_003051.4(RMRP):n.66T>C
NR_003051.4(RMRP):n.6C>A rs772443941
NR_003051.4(RMRP):n.6C>G
NR_003051.4(RMRP):n.70_71insT
NR_003051.4(RMRP):n.72A>T
NR_003051.4(RMRP):n.87C>T rs545284014
NR_003051.4(RMRP):n.91C>G
NR_003051.4(RMRP):n.92_93delAGinsGC rs387906533

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