rs369384363

Orientation

plus

Stabilized

plus

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

Make rs369384363(A;A)

Make rs369384363(A;G)

Reference

GRCh38 38.1/141

Chromosome

14

Position

91338121

Gene

CCDC88C

is a	snp
is	mentioned by
dbSNP	rs369384363
dbSNP (classic)	rs369384363
ClinGen	rs369384363
ebi	rs369384363
HLI	rs369384363
Exac	rs369384363
Gnomad	rs369384363
Varsome	rs369384363
LitVar	rs369384363
Map	rs369384363
PheGenI	rs369384363
Biobank	rs369384363
1000 genomes	rs369384363
hgdp	rs369384363
ensembl	rs369384363
geneview	rs369384363
scholar	rs369384363
google	rs369384363
pharmgkb	rs369384363
gwascentral	rs369384363
openSNP	rs369384363
23andMe	rs369384363
SNPshot	rs369384363
SNPdbe	rs369384363
MSV3d	rs369384363
GWAS Ctlg	rs369384363

Max Magnitude

0

ClinVar
Risk	rs369384363(A;A) rs369384363(C;C)
Alt	rs369384363(A;A) rs369384363(C;C)
Reference	Rs369384363(G;G)
Significance	Pathogenic
Disease	Hydrocephalus not specified
Variation	info
Gene	CCDC88C
CLNDBN	Hydrocephalus not specified
Reversed	0
HGVS	NC_000014.8:g.91804465G>A; NC_000014.8:g.91804465G>C
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000033088.4, RCV000483064.1,