rs878853098

Orientation

minus

Stabilized

minus

Geno	Mag	Summary
(GGAGATGCTTGTG;GGAGATGCTTGTG)	0	common in clinvar

Make rs878853098(-;-)

Make rs878853098(-;GGAGATGCTTGTG)

Reference

GRCh38.p2 38.2/147

Chromosome

19

Position

18786255

Gene

COMP

is a	snp
is	mentioned by
dbSNP	rs878853098
dbSNP (classic)	rs878853098
ClinGen	rs878853098
ebi	rs878853098
HLI	rs878853098
Exac	rs878853098
Gnomad	rs878853098
Varsome	rs878853098
LitVar	rs878853098
Map	rs878853098
PheGenI	rs878853098
Biobank	rs878853098
1000 genomes	rs878853098
hgdp	rs878853098
ensembl	rs878853098
geneview	rs878853098
scholar	rs878853098
google	rs878853098
pharmgkb	rs878853098
gwascentral	rs878853098
openSNP	rs878853098
23andMe	rs878853098
SNPshot	rs878853098
SNPdbe	rs878853098
MSV3d	rs878853098
GWAS Ctlg	rs878853098

Max Magnitude

0

ClinVar
Risk	rs878853098(-;-)
Alt	rs878853098(-;-)
Reference	Rs878853098(GGAGATGCTTGTG;GGAGATGCTTGTG)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	COMP
CLNDBN	not provided
Reversed	1
HGVS	NC_000019.9:g.18897065_18897077delCACAAGCATCTCC
CLNSRC
CLNACC	RCV000224737.1,