rs863225221

Orientation

plus

Stabilized

plus

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

Make rs863225221(G;T)

Make rs863225221(T;T)

Reference

GRCh38.p2 38.2/146

Chromosome

12

Position

123695276

Gene

TCTN2

is a	snp
is	mentioned by
dbSNP	rs863225221
dbSNP (classic)	rs863225221
ClinGen	rs863225221
ebi	rs863225221
HLI	rs863225221
Exac	rs863225221
Gnomad	rs863225221
Varsome	rs863225221
LitVar	rs863225221
Map	rs863225221
PheGenI	rs863225221
Biobank	rs863225221
1000 genomes	rs863225221
hgdp	rs863225221
ensembl	rs863225221
geneview	rs863225221
scholar	rs863225221
google	rs863225221
pharmgkb	rs863225221
gwascentral	rs863225221
openSNP	rs863225221
23andMe	rs863225221
SNPshot	rs863225221
SNPdbe	rs863225221
MSV3d	rs863225221
GWAS Ctlg	rs863225221

Max Magnitude

0

ClinVar
Risk	rs863225221(T;T)
Alt	rs863225221(T;T)
Reference	Rs863225221(G;G)
Significance	Pathogenic
Disease	Joubert syndrome
Variation	info
Gene	TCTN2
CLNDBN	Joubert syndrome
Reversed	0
HGVS	NC_000012.11:g.124179823G>T
CLNSRC
CLNACC	RCV000201712.1,