List of variants in gene GIPC3 reported as likely benign by GeneDx

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: 26

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HGVS	dbSNP	gnomAD frequency
NM_133261.3(GIPC3):c.593-151G>A	rs116092698	0.01368
NM_133261.3(GIPC3):c.787+43G>A	rs114801367	0.01137
NM_133261.3(GIPC3):c.593-167C>T	rs74364412	0.00481
NM_133261.3(GIPC3):c.*83G>A	rs543815063	0.00360
NM_133261.3(GIPC3):c.592+279T>C	rs374671510	0.00354
NM_133261.3(GIPC3):c.225+11C>T	rs185551765	0.00351
NM_133261.3(GIPC3):c.132G>C (p.Ala44=)	rs80060313	0.00180
NM_133261.3(GIPC3):c.856G>A (p.Val286Ile)	rs138339125	0.00121
NM_133261.3(GIPC3):c.4G>A (p.Glu2Lys)	rs764467903	0.00110
NM_133261.3(GIPC3):c.788-45C>T	rs370162131	0.00050
NM_133261.3(GIPC3):c.592+10G>T	rs557737423	0.00042
NM_133261.3(GIPC3):c.20G>A (p.Arg7Gln)	rs998073430	0.00028
NM_133261.3(GIPC3):c.807G>A (p.Thr269=)	rs141419242	0.00017
NM_133261.3(GIPC3):c.788-43C>T	rs35385787	0.00015
NM_133261.3(GIPC3):c.871G>A (p.Ala291Thr)	rs199951984	0.00009
NM_133261.3(GIPC3):c.639G>A (p.Ala213=)	rs371566042	0.00008
NM_133261.3(GIPC3):c.411+25G>A	rs557145939	0.00006
NM_133261.3(GIPC3):c.788-4G>A	rs372583605	0.00006
NM_133261.3(GIPC3):c.592+7C>T	rs537708164	0.00002
NM_133261.3(GIPC3):c.*15del	rs761229176
NM_133261.3(GIPC3):c.-46G>C	rs545605260
NM_133261.3(GIPC3):c.411+10A>G	rs779727957
NM_133261.3(GIPC3):c.411+55dup	rs531054314
NM_133261.3(GIPC3):c.69G>A (p.Ala23=)	rs150473323
NM_133261.3(GIPC3):c.69G>C (p.Ala23=)	rs150473323
NM_133261.3(GIPC3):c.821C>T (p.Ala274Val)	rs149028750

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