rs863225222

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(-;-)	0	common in clinvar
(D;D)	0	common genotype

Make rs863225222(-;G)

Make rs863225222(G;G)

Reference

GRCh38.p2 38.2/146

Chromosome

12

Position

123671316

Gene

TCTN2

is a	snp
is	mentioned by
dbSNP	rs863225222
dbSNP (classic)	rs863225222
ClinGen	rs863225222
ebi	rs863225222
HLI	rs863225222
Exac	rs863225222
Gnomad	rs863225222
Varsome	rs863225222
LitVar	rs863225222
Map	rs863225222
PheGenI	rs863225222
Biobank	rs863225222
1000 genomes	rs863225222
hgdp	rs863225222
ensembl	rs863225222
geneview	rs863225222
scholar	rs863225222
google	rs863225222
pharmgkb	rs863225222
gwascentral	rs863225222
openSNP	rs863225222
23andMe	rs863225222
SNPshot	rs863225222
SNPdbe	rs863225222
MSV3d	rs863225222
GWAS Ctlg	rs863225222

Max Magnitude

0

ClinVar
Risk	rs863225222(G;G)
Alt	rs863225222(G;G)
Reference	Rs863225222(-;-)
Significance	Pathogenic
Disease	Joubert syndrome Joubert syndrome 24
Variation	info
Gene	TCTN2
CLNDBN	Joubert syndrome Joubert syndrome 24
Reversed	0
HGVS	NC_000012.11:g.124155863dupG
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000201539.1, RCV000202326.1,