rs121909086

Orientation

minus

Stabilized

minus

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

Make rs121909086(C;T)

Make rs121909086(T;T)

Reference

GRCh38 38.1/141

Chromosome

9

Position

91737400

Gene

ROR2

is a	snp
is	mentioned by
dbSNP	rs121909086
dbSNP (classic)	rs121909086
ClinGen	rs121909086
ebi	rs121909086
HLI	rs121909086
Exac	rs121909086
Gnomad	rs121909086
Varsome	rs121909086
LitVar	rs121909086
Map	rs121909086
PheGenI	rs121909086
Biobank	rs121909086
1000 genomes	rs121909086
hgdp	rs121909086
ensembl	rs121909086
geneview	rs121909086
scholar	rs121909086
google	rs121909086
pharmgkb	rs121909086
gwascentral	rs121909086
openSNP	rs121909086
23andMe	rs121909086
SNPshot	rs121909086
SNPdbe	rs121909086
MSV3d	rs121909086
GWAS Ctlg	rs121909086

Max Magnitude

0

OMIM	602337
Desc
Variant	0007
Related	also

ClinVar
Risk	rs121909086(A;A) rs121909086(T;T)
Alt	rs121909086(A;A) rs121909086(T;T)
Reference	Rs121909086(C;C)
Significance	Pathogenic
Disease	Robinow syndrome
Variation	info
Gene	ROR2
CLNDBN	Robinow syndrome, autosomal recessive
Reversed	1
HGVS	NC_000009.11:g.94499682G>A
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000007733.4,