rs786205622

Orientation

plus

Stabilized

plus

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

Make rs786205622(-;-)

Make rs786205622(-;TG)

Reference

GRCh38.p2 38.2/146

Chromosome

12

Position

123672117

Gene

TCTN2

is a	snp
is	mentioned by
dbSNP	rs786205622
dbSNP (classic)	rs786205622
ClinGen	rs786205622
ebi	rs786205622
HLI	rs786205622
Exac	rs786205622
Gnomad	rs786205622
Varsome	rs786205622
LitVar	rs786205622
Map	rs786205622
PheGenI	rs786205622
Biobank	rs786205622
1000 genomes	rs786205622
hgdp	rs786205622
ensembl	rs786205622
geneview	rs786205622
scholar	rs786205622
google	rs786205622
pharmgkb	rs786205622
gwascentral	rs786205622
openSNP	rs786205622
23andMe	rs786205622
SNPshot	rs786205622
SNPdbe	rs786205622
MSV3d	rs786205622
GWAS Ctlg	rs786205622

Max Magnitude

0

ClinVar
Risk	rs786205622(-;-)
Alt	rs786205622(-;-)
Reference	Rs786205622(TG;TG)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	TCTN2
CLNDBN	not provided
Reversed	0
HGVS	NC_000012.11:g.124156664_124156665delTG
CLNSRC
CLNACC	RCV000171472.1,