rs863225181

Orientation

plus

Stabilized

plus

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

Make rs863225181(A;A)

Make rs863225181(A;G)

Reference

GRCh38.p2 38.2/146

Chromosome

4

Position

15570501

Gene

CC2D2A

is a	snp
is	mentioned by
dbSNP	rs863225181
dbSNP (classic)	rs863225181
ClinGen	rs863225181
ebi	rs863225181
HLI	rs863225181
Exac	rs863225181
Gnomad	rs863225181
Varsome	rs863225181
LitVar	rs863225181
Map	rs863225181
PheGenI	rs863225181
Biobank	rs863225181
1000 genomes	rs863225181
hgdp	rs863225181
ensembl	rs863225181
geneview	rs863225181
scholar	rs863225181
google	rs863225181
pharmgkb	rs863225181
gwascentral	rs863225181
openSNP	rs863225181
23andMe	rs863225181
SNPshot	rs863225181
SNPdbe	rs863225181
MSV3d	rs863225181
GWAS Ctlg	rs863225181

Max Magnitude

0

ClinVar
Risk	rs863225181(A;A)
Alt	rs863225181(A;A)
Reference	Rs863225181(G;G)
Significance	Probable-Pathogenic
Disease	Joubert syndrome 9 not specified
Variation	info
Gene	CC2D2A
CLNDBN	Joubert syndrome 9 not specified
Reversed	0
HGVS	NC_000004.11:g.15572124G>A
CLNSRC
CLNACC	RCV000201770.1, RCV000319494.1,