rs869025222

Orientation

plus

Stabilized

plus

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

Make rs869025222(C;C)

Make rs869025222(C;T)

Reference

GRCh38.p2 38.2/147

Chromosome

3

Position

25580574

Gene

RARB

is a	snp
is	mentioned by
dbSNP	rs869025222
dbSNP (classic)	rs869025222
ClinGen	rs869025222
ebi	rs869025222
HLI	rs869025222
Exac	rs869025222
Gnomad	rs869025222
Varsome	rs869025222
LitVar	rs869025222
Map	rs869025222
PheGenI	rs869025222
Biobank	rs869025222
1000 genomes	rs869025222
hgdp	rs869025222
ensembl	rs869025222
geneview	rs869025222
scholar	rs869025222
google	rs869025222
pharmgkb	rs869025222
gwascentral	rs869025222
openSNP	rs869025222
23andMe	rs869025222
SNPshot	rs869025222
SNPdbe	rs869025222
MSV3d	rs869025222
GWAS Ctlg	rs869025222

Max Magnitude

0

ClinVar
Risk	rs869025222(C;C)
Alt	rs869025222(C;C)
Reference	Rs869025222(T;T)
Significance	Probable-Pathogenic
Disease	Microphthalmia
Variation	info
Gene	RARB
CLNDBN	Microphthalmia, syndromic 12
Reversed	0
HGVS	NC_000003.11:g.25622065T>C
CLNSRC
CLNACC	RCV000207485.1,