List of variants in gene PIGM reported as likely benign for blood coagulation disease

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 10

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HGVS	dbSNP	gnomAD frequency
NM_145167.3(PIGM):c.1017C>T (p.Tyr339=)	rs200046659	0.00019
NM_145167.3(PIGM):c.183C>T (p.Phe61=)	rs745664346	0.00001
NM_145167.3(PIGM):c.294C>T (p.Leu98=)	rs750695305	0.00001
NM_145167.3(PIGM):c.438G>A (p.Ala146=)	rs772665564	0.00001
NM_145167.3(PIGM):c.696A>G (p.Ala232=)	rs1648314579	0.00001
NM_145167.3(PIGM):c.1143A>G (p.Gln381=)
NM_145167.3(PIGM):c.129G>A (p.Leu43=)
NM_145167.3(PIGM):c.189G>C (p.Thr63=)
NM_145167.3(PIGM):c.216C>A (p.Ala72=)
NM_145167.3(PIGM):c.867C>G (p.Ser289=)	rs776974327

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