rs104894663

Orientation

minus

Stabilized

minus

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

Make rs104894663(C;T)

Make rs104894663(T;T)

Reference

GRCh38 38.1/141

Chromosome

18

Position

59272465

Gene

RAX

is a	snp
is	mentioned by
dbSNP	rs104894663
dbSNP (classic)	rs104894663
ClinGen	rs104894663
ebi	rs104894663
HLI	rs104894663
Exac	rs104894663
Gnomad	rs104894663
Varsome	rs104894663
LitVar	rs104894663
Map	rs104894663
PheGenI	rs104894663
Biobank	rs104894663
1000 genomes	rs104894663
hgdp	rs104894663
ensembl	rs104894663
geneview	rs104894663
scholar	rs104894663
google	rs104894663
pharmgkb	rs104894663
gwascentral	rs104894663
openSNP	rs104894663
23andMe	rs104894663
SNPshot	rs104894663
SNPdbe	rs104894663
MSV3d	rs104894663
GWAS Ctlg	rs104894663

Max Magnitude

0

OMIM	601881
Desc
Variant	0001
Related	also

ClinVar
Risk	rs104894663(T;T)
Alt	rs104894663(T;T)
Reference	Rs104894663(C;C)
Significance	Pathogenic
Disease	Microphthalmia
Variation	info
Gene	RAX
CLNDBN	Microphthalmia, isolated 3
Reversed	1
HGVS	NC_000018.9:g.56939697G>A
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000008074.4,