rs863225425

Orientation

plus

Stabilized

plus

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

Make rs863225425(A;A)

Make rs863225425(A;G)

Reference

GRCh38.p2 38.2/146

Chromosome

12

Position

123695219

Gene

TCTN2

is a	snp
is	mentioned by
dbSNP	rs863225425
dbSNP (classic)	rs863225425
ClinGen	rs863225425
ebi	rs863225425
HLI	rs863225425
Exac	rs863225425
Gnomad	rs863225425
Varsome	rs863225425
LitVar	rs863225425
Map	rs863225425
PheGenI	rs863225425
Biobank	rs863225425
1000 genomes	rs863225425
hgdp	rs863225425
ensembl	rs863225425
geneview	rs863225425
scholar	rs863225425
google	rs863225425
pharmgkb	rs863225425
gwascentral	rs863225425
openSNP	rs863225425
23andMe	rs863225425
SNPshot	rs863225425
SNPdbe	rs863225425
MSV3d	rs863225425
GWAS Ctlg	rs863225425

Max Magnitude

0

ClinVar
Risk	rs863225425(A;A)
Alt	rs863225425(A;A)
Reference	Rs863225425(G;G)
Significance	Pathogenic
Disease	Joubert syndrome 24
Variation	info
Gene	TCTN2
CLNDBN	Joubert syndrome 24
Reversed	0
HGVS	NC_000012.11:g.124179766G>A
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000202333.1,