List of variants in gene RARS2 reported as likely benign for not specified

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: 29

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_020320.5(RARS2):c.872A>G (p.Lys291Arg)	rs17850652	0.09110
NM_020320.5(RARS2):c.991A>G (p.Ile331Val)	rs3757370	0.02330
NM_020320.5(RARS2):c.606C>T (p.Leu202=)	rs75794097	0.01095
NM_020320.5(RARS2):c.-8A>C	rs28381459	0.00245
NM_020320.5(RARS2):c.1410C>A (p.Leu470=)	rs139564081	0.00223
NM_020320.5(RARS2):c.456T>C (p.Asn152=)	rs141374913	0.00070
NM_020320.5(RARS2):c.207A>G (p.Ala69=)	rs568483789	0.00025
NM_020320.5(RARS2):c.318T>A (p.Ile106=)	rs758445993	0.00007
NM_020320.5(RARS2):c.1338G>C (p.Lys446Asn)	rs144988947	0.00006
NM_020320.5(RARS2):c.1287C>T (p.Leu429=)	rs192821560	0.00005
NM_020320.5(RARS2):c.111-15G>A	rs1046165044	0.00003
NM_020320.5(RARS2):c.1221C>A (p.Asn407Lys)	rs760831364	0.00003
NM_020320.5(RARS2):c.9C>T (p.Cys3=)	rs762495974	0.00003
NM_020320.5(RARS2):c.-13C>T	rs200228607	0.00002
NM_020320.5(RARS2):c.-12G>A	rs768137659	0.00001
NM_020320.5(RARS2):c.1263A>G (p.Gln421=)	rs767004280	0.00001
NM_020320.5(RARS2):c.536-7A>G	rs906902972	0.00001
NM_020320.5(RARS2):c.688T>C (p.Leu230=)	rs781045597	0.00001
NM_020320.5(RARS2):c.155A>G (p.Lys52Arg)	rs73496064
NM_020320.5(RARS2):c.1651-14_1651-10del	rs763164942
NM_020320.5(RARS2):c.196A>G (p.Lys66Glu)	rs863224177
NM_020320.5(RARS2):c.294A>C (p.Thr98=)	rs1237155881
NM_020320.5(RARS2):c.395+14C>T	rs1057523578
NM_020320.5(RARS2):c.451+9T>C	rs778200533
NM_020320.5(RARS2):c.452-22TA[2]	rs772255685
NM_020320.5(RARS2):c.588C>T (p.Ser196=)	rs1057523360
NM_020320.5(RARS2):c.641C>T (p.Ala214Val)	rs863224178
NM_020320.5(RARS2):c.726A>G (p.Gln242=)	rs145499324
NM_020320.5(RARS2):c.772-4T>G	rs1413353465

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.