rs104894113

Orientation

plus

Stabilized

plus

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

Make rs104894113(G;T)

Make rs104894113(T;T)

Reference

GRCh37 37.1/132

Chromosome

9

Position

2718166

Gene

KCNV2

is a	snp
is	mentioned by
dbSNP	rs104894113
dbSNP (classic)	rs104894113
ClinGen	rs104894113
ebi	rs104894113
HLI	rs104894113
Exac	rs104894113
Gnomad	rs104894113
Varsome	rs104894113
LitVar	rs104894113
Map	rs104894113
PheGenI	rs104894113
Biobank	rs104894113
1000 genomes	rs104894113
hgdp	rs104894113
ensembl	rs104894113
geneview	rs104894113
scholar	rs104894113
google	rs104894113
pharmgkb	rs104894113
gwascentral	rs104894113
openSNP	rs104894113
23andMe	rs104894113
SNPshot	rs104894113
SNPdbe	rs104894113
MSV3d	rs104894113
GWAS Ctlg	rs104894113

Max Magnitude

0

OMIM	607604
Desc
Variant	0001
Related	also

ClinVar
Risk	rs104894113(A;A) rs104894113(T;T)
Alt	rs104894113(A;A) rs104894113(T;T)
Reference	Rs104894113(G;G)
Significance	Pathogenic
Disease	Retinal cone dystrophy 3B
Variation	info
Gene	KCNV2
CLNDBN	Retinal cone dystrophy 3B
Reversed	0
HGVS	NC_000009.11:g.2718166G>T
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000003146.2,