rs16892095

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(A;A)	0	common genotype

Make rs16892095(A;C)

Make rs16892095(C;C)

Reference

GRCh38.p2 38.2/144

Chromosome

4

Position

15516734

Gene

CC2D2A

is a	snp
is	mentioned by
dbSNP	rs16892095
dbSNP (classic)	rs16892095
ClinGen	rs16892095
ebi	rs16892095
HLI	rs16892095
Exac	rs16892095
Gnomad	rs16892095
Varsome	rs16892095
LitVar	rs16892095
Map	rs16892095
PheGenI	rs16892095
Biobank	rs16892095
1000 genomes	rs16892095
hgdp	rs16892095
ensembl	rs16892095
geneview	rs16892095
scholar	rs16892095
google	rs16892095
pharmgkb	rs16892095
gwascentral	rs16892095
openSNP	rs16892095
23andMe	rs16892095
SNPshot	rs16892095
SNPdbe	rs16892095
MSV3d	rs16892095
GWAS Ctlg	rs16892095

Max Magnitude

0

?	(A;A) (A;C) (C;C)	28

ClinVar
Risk	rs16892095(C;C)
Alt	rs16892095(C;C)
Reference	Rs16892095(A;A)
Significance	Other
Disease	not specified Meckel-Gruber syndrome Joubert syndrome
Variation	info
Gene	CC2D2A
CLNDBN	not specified Meckel-Gruber syndrome Joubert syndrome
Reversed	0
HGVS	NC_000004.11:g.15518357A>C
CLNSRC	UniProtKB (protein)
CLNACC	RCV000114163.4, RCV000322215.1, RCV000379834.1,