rs863225426

Orientation

plus

Stabilized

plus

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

Make rs863225426(C;T)

Make rs863225426(T;T)

Reference

GRCh38.p2 38.2/146

Chromosome

12

Position

123706829

Gene

TCTN2

is a	snp
is	mentioned by
dbSNP	rs863225426
dbSNP (classic)	rs863225426
ClinGen	rs863225426
ebi	rs863225426
HLI	rs863225426
Exac	rs863225426
Gnomad	rs863225426
Varsome	rs863225426
LitVar	rs863225426
Map	rs863225426
PheGenI	rs863225426
Biobank	rs863225426
1000 genomes	rs863225426
hgdp	rs863225426
ensembl	rs863225426
geneview	rs863225426
scholar	rs863225426
google	rs863225426
pharmgkb	rs863225426
gwascentral	rs863225426
openSNP	rs863225426
23andMe	rs863225426
SNPshot	rs863225426
SNPdbe	rs863225426
MSV3d	rs863225426
GWAS Ctlg	rs863225426

Max Magnitude

0

ClinVar
Risk	rs863225426(T;T)
Alt	rs863225426(T;T)
Reference	Rs863225426(C;C)
Significance	Pathogenic
Disease	Joubert syndrome 24
Variation	info
Gene	TCTN2
CLNDBN	Joubert syndrome 24
Reversed	0
HGVS	NC_000012.11:g.124191376C>T
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000202341.1,