rs1045644

Orientation

plus

Stabilized

plus

Make rs1045644(C;G)

Make rs1045644(G;G)

Reference

GRCh38 38.1/141

Chromosome

14

Position

30885890

Gene	COCH, LOC100506071

is a	snp
is	mentioned by
dbSNP	rs1045644
dbSNP (classic)	rs1045644
ClinGen	rs1045644
ebi	rs1045644
HLI	rs1045644
Exac	rs1045644
Gnomad	rs1045644
Varsome	rs1045644
LitVar	rs1045644
Map	rs1045644
PheGenI	rs1045644
Biobank	rs1045644
1000 genomes	rs1045644
hgdp	rs1045644
ensembl	rs1045644
geneview	rs1045644
scholar	rs1045644
google	rs1045644
pharmgkb	rs1045644
gwascentral	rs1045644
openSNP	rs1045644
23andMe	rs1045644
SNPshot	rs1045644
SNPdbe	rs1045644
MSV3d	rs1045644
GWAS Ctlg	rs1045644

GMAF

0.4665

Max Magnitude

0

?	(C;C) (C;G) (G;G)	28

[PMID 18520591] Sequence variants in host cell factor C1 are associated with Meniere's disease.

ClinVar
Risk	rs1045644(G;G)
Alt	rs1045644(G;G)
Reference	Rs1045644(C;C)
Significance	Non-pathogenic
Disease	not specified Nonsyndromic Hearing Loss
Variation	info
Gene	COCH LOC100506071
CLNDBN	not specified Nonsyndromic Hearing Loss, Dominant
Reversed	0
HGVS	NC_000014.8:g.31355096C>G
CLNSRC
CLNACC	RCV000221727.2, RCV000290341.1,