rs121909087

Orientation

minus

Stabilized

minus

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

Make rs121909087(C;T)

Make rs121909087(T;T)

Reference

GRCh38 38.1/141

Chromosome

9

Position

91757380

Gene

ROR2

is a	snp
is	mentioned by
dbSNP	rs121909087
dbSNP (classic)	rs121909087
ClinGen	rs121909087
ebi	rs121909087
HLI	rs121909087
Exac	rs121909087
Gnomad	rs121909087
Varsome	rs121909087
LitVar	rs121909087
Map	rs121909087
PheGenI	rs121909087
Biobank	rs121909087
1000 genomes	rs121909087
hgdp	rs121909087
ensembl	rs121909087
geneview	rs121909087
scholar	rs121909087
google	rs121909087
pharmgkb	rs121909087
gwascentral	rs121909087
openSNP	rs121909087
23andMe	rs121909087
SNPshot	rs121909087
SNPdbe	rs121909087
MSV3d	rs121909087
GWAS Ctlg	rs121909087

Max Magnitude

0

OMIM	602337
Desc
Variant	0011
Related	also

ClinVar
Risk	rs121909087(T;T)
Alt	rs121909087(T;T)
Reference	Rs121909087(C;C)
Significance	Pathogenic
Disease	Robinow syndrome not provided
Variation	info
Gene	ROR2
CLNDBN	Robinow syndrome, autosomal recessive not provided
Reversed	1
HGVS	NC_000009.11:g.94519662G>A
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000007738.4, RCV000238984.1,