List of variants in gene GP1BA reported as pathogenic 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)
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Total variants: 8

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HGVS	dbSNP	gnomAD frequency
NM_000173.7(GP1BA):c.1326_1334del (p.Glu442_Pro445delinsAsp)	rs2151108403
NM_000173.7(GP1BA):c.515C>T (p.Ala172Val)	rs121908065
NM_000173.7(GP1BA):c.737G>T (p.Trp246Leu)	rs2151107964
NM_000173.7(GP1BA):c.746G>A (p.Gly249Asp)	rs121908062
NM_000173.7(GP1BA):c.746G>T (p.Gly249Val)	rs121908062
NM_000173.7(GP1BA):c.763A>G (p.Met255Val)	rs121908064
NM_000173.7(GP1BA):c.793G>T (p.Asp265Tyr)	rs765474118
NM_000173.7(GP1BA):c.987G>A (p.Trp329Ter)

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