List of variants reported as uncertain significance for adenocarcinoma by CSER _CC_NCGL, University of Washington

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 8

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_003000.3(SDHB):c.32G>A (p.Arg11His)	rs111430410	0.00185
NM_004360.5(CDH1):c.2104G>A (p.Glu702Lys)	rs149127230	0.00058
NM_004360.5(CDH1):c.2413G>A (p.Asp805Asn)	rs200894246	0.00026
NM_020975.6(RET):c.1531G>A (p.Glu511Lys)	rs201553718	0.00018
NM_020975.6(RET):c.961G>A (p.Gly321Arg)	rs377767388	0.00009
NM_000251.3(MSH2):c.1045C>G (p.Pro349Ala)	rs267607939	0.00007
NM_020975.6(RET):c.2452G>A (p.Glu818Lys)	rs377767420	0.00003
NM_020975.6(RET):c.2656C>T (p.Arg886Trp)	rs146838520	0.00003

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.