rs104894480

Orientation

plus

Stabilized

plus

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

Make rs104894480(A;G)

Make rs104894480(G;G)

Reference

GRCh38 38.1/141

Chromosome

14

Position

60509891

Gene

SIX6

is a	snp
is	mentioned by
dbSNP	rs104894480
dbSNP (classic)	rs104894480
ClinGen	rs104894480
ebi	rs104894480
HLI	rs104894480
Exac	rs104894480
Gnomad	rs104894480
Varsome	rs104894480
LitVar	rs104894480
Map	rs104894480
PheGenI	rs104894480
Biobank	rs104894480
1000 genomes	rs104894480
hgdp	rs104894480
ensembl	rs104894480
geneview	rs104894480
scholar	rs104894480
google	rs104894480
pharmgkb	rs104894480
gwascentral	rs104894480
openSNP	rs104894480
23andMe	rs104894480
SNPshot	rs104894480
SNPdbe	rs104894480
MSV3d	rs104894480
GWAS Ctlg	rs104894480

Max Magnitude

0

OMIM	606326
Desc
Variant	0001
Related	also

ClinVar
Risk	rs104894480(G;G)
Alt	rs104894480(G;G)
Reference	Rs104894480(A;A)
Significance	Pathogenic
Disease	Cataract
Variation	info
Gene	SIX6
CLNDBN	Cataract, microphthalmia and nystagmus
Reversed	0
HGVS	NC_000014.8:g.60976609A>G
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000004686.4,