rs121909083

Orientation

minus

Stabilized

minus

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

Make rs121909083(C;T)

Make rs121909083(T;T)

Reference

GRCh38 38.1/141

Chromosome

9

Position

91724990

Gene

ROR2

is a	snp
is	mentioned by
dbSNP	rs121909083
dbSNP (classic)	rs121909083
ClinGen	rs121909083
ebi	rs121909083
HLI	rs121909083
Exac	rs121909083
Gnomad	rs121909083
Varsome	rs121909083
LitVar	rs121909083
Map	rs121909083
PheGenI	rs121909083
Biobank	rs121909083
1000 genomes	rs121909083
hgdp	rs121909083
ensembl	rs121909083
geneview	rs121909083
scholar	rs121909083
google	rs121909083
pharmgkb	rs121909083
gwascentral	rs121909083
openSNP	rs121909083
23andMe	rs121909083
SNPshot	rs121909083
SNPdbe	rs121909083
MSV3d	rs121909083
GWAS Ctlg	rs121909083

Max Magnitude

0

OMIM	602337
Desc
Variant	0004
Related	also

ClinVar
Risk	rs121909083(T;T)
Alt	rs121909083(T;T)
Reference	Rs121909083(C;C)
Significance	Pathogenic
Disease	Robinow syndrome
Variation	info
Gene	ROR2
CLNDBN	Robinow syndrome, autosomal recessive
Reversed	1
HGVS	NC_000009.11:g.94487272G>A
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000007730.3,