List of intergenic variants reported as benign by ISCA site 8

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: 15

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
GRCh37/hg19 10q11.22(chr10:47006954-47074861)x1
GRCh37/hg19 1q21.1(chr1:144451745-144524956)x3
GRCh37/hg19 Yq12(chrY:59002344-59031480)x2
GRCh38/hg38 10q26.3(chr10:133577759-133597879)x3
GRCh38/hg38 14q21.2(chr14:45352239-45510526)x1
GRCh38/hg38 16p13.11(chr16:16431432-16678513)x1
GRCh38/hg38 1q31.1(chr1:188236818-188605371)x1
GRCh38/hg38 1q31.1(chr1:189460972-189593144)x1
GRCh38/hg38 7p14.1(chr7:41184839-41403900)x1
GRCh38/hg38 7q31.31(chr7:119226617-119374558)x1
GRCh38/hg38 8q11.1(chr8:46031334-46662449)x1
GRCh38/hg38 Xp22.31(chrX:7515855-7666651)x2
GRCh38/hg38 Xq11.1(chrX:62779286-62913742)x2
NCBI36/hg18 1q21.1(chr1:142444242-142683157)x1
NCBI36/hg18 7q11.23(chr7:74381487-74594440)x3

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.