List of variants in gene combination GCDH, LOC126862860, SYCE2 reported by Counsyl

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 10

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_000159.4(GCDH):c.*101G>A	rs140251161	0.00067
NM_000159.4(GCDH):c.1261G>A (p.Ala421Thr)	rs151201155	0.00061
NM_000159.4(GCDH):c.1244-15A>G	rs201407990	0.00014
NM_000159.4(GCDH):c.1298C>T (p.Ala433Val)	rs933624223	0.00002
NM_000159.4(GCDH):c.1315T>C (p.Ter439Arg)	rs771126053	0.00002
NM_000159.4(GCDH):c.*201A>C	rs1356787323	0.00001
NM_000159.4(GCDH):c.1286C>T (p.Thr429Met)	rs745360675	0.00001
NM_000159.4(GCDH):c.*182AGA[1]	rs1555752085
NM_000159.4(GCDH):c.1244-2A>G	rs199999619
NM_000159.4(GCDH):c.1317A>G (p.Ter439Trp)	rs1555751995

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.