ClinVar Miner

List of variants in gene PARN reported as uncertain significance for anemia (disease)

Included ClinVar conditions (263):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 24
Download table as spreadsheet
HGVS dbSNP
NM_002582.4(PARN):c.1219C>G (p.His407Asp)
NM_002582.4(PARN):c.1297C>G (p.Leu433Val)
NM_002582.4(PARN):c.1351A>G (p.Thr451Ala)
NM_002582.4(PARN):c.1405+3A>G
NM_002582.4(PARN):c.1493G>A (p.Ser498Asn)
NM_002582.4(PARN):c.1501G>T (p.Ala501Ser)
NM_002582.4(PARN):c.1613G>C (p.Arg538Pro) rs377199187
NM_002582.4(PARN):c.1650T>A (p.Asn550Lys)
NM_002582.4(PARN):c.1661G>A (p.Arg554His)
NM_002582.4(PARN):c.1697A>G (p.Lys566Arg) rs1567284498
NM_002582.4(PARN):c.1785T>G (p.Asp595Glu)
NM_002582.4(PARN):c.1789T>C (p.Cys597Arg)
NM_002582.4(PARN):c.1842G>A (p.Met614Ile)
NM_002582.4(PARN):c.1843A>G (p.Lys615Glu) rs368440052
NM_002582.4(PARN):c.271T>A (p.Tyr91Asn)
NM_002582.4(PARN):c.272A>G (p.Tyr91Cys) rs201765587
NM_002582.4(PARN):c.34C>T (p.Leu12Phe)
NM_002582.4(PARN):c.407A>T (p.Gln136Leu)
NM_002582.4(PARN):c.449G>A (p.Arg150His)
NM_002582.4(PARN):c.466G>T (p.Ala156Ser)
NM_002582.4(PARN):c.702+5C>T
NM_002582.4(PARN):c.7A>G (p.Ile3Val) rs1567474981
NM_002582.4(PARN):c.853A>G (p.Ile285Val)
NM_002582.4(PARN):c.924A>C (p.Leu308Phe)

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.