List of variants in gene GCDH reported as uncertain significance by Counsyl

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: 27

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HGVS	dbSNP	gnomAD frequency
NM_000159.4(GCDH):c.428T>C (p.Val143Ala)	rs141456457	0.00004
NM_000159.4(GCDH):c.1144G>A (p.Ala382Thr)	rs567564095	0.00003
NM_000159.4(GCDH):c.1148G>A (p.Arg383His)	rs764608975	0.00003
NM_000159.4(GCDH):c.536T>G (p.Leu179Arg)	rs774526353	0.00002
NM_000159.4(GCDH):c.641C>T (p.Thr214Met)	rs1131692030	0.00002
NM_000159.4(GCDH):c.1015A>G (p.Met339Val)	rs752234195	0.00001
NM_000159.4(GCDH):c.365C>T (p.Ala122Val)	rs766325846	0.00001
NM_000159.4(GCDH):c.479A>G (p.Gln160Arg)	rs1176799813	0.00001
NM_000159.4(GCDH):c.852+5G>A	rs886054243	0.00001
NM_000159.4(GCDH):c.873C>A (p.Asn291Lys)	rs1328059662	0.00001
NM_000159.4(GCDH):c.910G>A (p.Ala304Thr)	rs373203481	0.00001
NM_000159.4(GCDH):c.1115G>A (p.Arg372Lys)	rs1555751240
NM_000159.4(GCDH):c.1169G>T (p.Gly390Val)	rs778153326
NM_000159.4(GCDH):c.1220T>C (p.Leu407Pro)	rs1555751379
NM_000159.4(GCDH):c.281G>A (p.Arg94Gln)	rs566417795
NM_000159.4(GCDH):c.380_391del (p.Ala127_Leu130del)	rs1555749893
NM_000159.4(GCDH):c.394C>G (p.Arg132Gly)	rs372429120
NM_000159.4(GCDH):c.397G>T (p.Val133Leu)	rs746388510
NM_000159.4(GCDH):c.416C>G (p.Ser139Trp)	rs139851890
NM_000159.4(GCDH):c.427G>A (p.Val143Ile)	rs1555749918
NM_000159.4(GCDH):c.437C>A (p.Ser146Tyr)	rs1555749927
NM_000159.4(GCDH):c.636-2dup	rs762345287
NM_000159.4(GCDH):c.640A>G (p.Thr214Ala)	rs1468636851
NM_000159.4(GCDH):c.700C>T (p.Arg234Trp)	rs964724051
NM_000159.4(GCDH):c.730G>A (p.Gly244Ser)	rs1555750589
NM_000159.4(GCDH):c.798G>A (p.Met266Ile)	rs1555750632
NM_000159.4(GCDH):c.997C>G (p.Gln333Glu)	rs794726972

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