rs786205489

Orientation

minus

Stabilized

minus

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

Make rs786205489(C;C)

Make rs786205489(C;G)

Reference

GRCh38.p2 38.2/146

Chromosome

14

Position

91291030

Gene

CCDC88C

is a	snp
is	mentioned by
dbSNP	rs786205489
dbSNP (classic)	rs786205489
ClinGen	rs786205489
ebi	rs786205489
HLI	rs786205489
Exac	rs786205489
Gnomad	rs786205489
Varsome	rs786205489
LitVar	rs786205489
Map	rs786205489
PheGenI	rs786205489
Biobank	rs786205489
1000 genomes	rs786205489
hgdp	rs786205489
ensembl	rs786205489
geneview	rs786205489
scholar	rs786205489
google	rs786205489
pharmgkb	rs786205489
gwascentral	rs786205489
openSNP	rs786205489
23andMe	rs786205489
SNPshot	rs786205489
SNPdbe	rs786205489
MSV3d	rs786205489
GWAS Ctlg	rs786205489

Max Magnitude

0

ClinVar
Risk	rs786205489(C;C)
Alt	rs786205489(C;C)
Reference	Rs786205489(G;G)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	CCDC88C
CLNDBN	not provided
Reversed	1
HGVS	NC_000014.8:g.91757374C>G
CLNSRC
CLNACC	RCV000171227.1,