List of variants in gene MPL reported as likely benign for MPL-related disorder

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: 13

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HGVS	dbSNP	gnomAD frequency
NM_005373.3(MPL):c.677C>A (p.Ser226Tyr)	rs141063159	0.00170
NM_005373.3(MPL):c.1488C>T (p.Thr496=)	rs140091584	0.00056
NM_005373.3(MPL):c.1570C>T (p.Leu524=)	rs146372205	0.00053
NM_005373.3(MPL):c.1336G>A (p.Gly446Arg)	rs561818288	0.00046
NM_005373.3(MPL):c.963G>T (p.Arg321=)	rs138636505	0.00024
NM_005373.3(MPL):c.549G>A (p.Thr183=)	rs147130173	0.00023
NM_005373.3(MPL):c.1063A>G (p.Lys355Glu)	rs546510242	0.00017
NM_005373.3(MPL):c.1467C>T (p.Thr489=)	rs759161511	0.00009
NM_005373.3(MPL):c.1446G>A (p.Arg482=)	rs1046680606	0.00006
NM_005373.3(MPL):c.1002C>T (p.Cys334=)	rs141526418	0.00005
NM_005373.3(MPL):c.1242G>A (p.Ser414=)	rs544064034	0.00002
NM_005373.3(MPL):c.120T>C (p.Cys40=)	rs747864027	0.00001
NM_005373.3(MPL):c.*10C>T	rs1042072149

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