rs267607016

Orientation

minus

Stabilized

minus

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

Make rs267607016(C;T)

Make rs267607016(T;T)

Reference

GRCh38 38.1/141

Chromosome

9

Position

91726603

Gene

ROR2

is a	snp
is	mentioned by
dbSNP	rs267607016
dbSNP (classic)	rs267607016
ClinGen	rs267607016
ebi	rs267607016
HLI	rs267607016
Exac	rs267607016
Gnomad	rs267607016
Varsome	rs267607016
LitVar	rs267607016
Map	rs267607016
PheGenI	rs267607016
Biobank	rs267607016
1000 genomes	rs267607016
hgdp	rs267607016
ensembl	rs267607016
geneview	rs267607016
scholar	rs267607016
google	rs267607016
pharmgkb	rs267607016
gwascentral	rs267607016
openSNP	rs267607016
23andMe	rs267607016
SNPshot	rs267607016
SNPdbe	rs267607016
MSV3d	rs267607016
GWAS Ctlg	rs267607016

Max Magnitude

0

ClinVar
Risk	rs267607016(T;T)
Alt	rs267607016(T;T)
Reference	Rs267607016(C;C)
Significance	Pathogenic
Disease	Robinow syndrome
Variation	info
Gene	ROR2
CLNDBN	Robinow syndrome, autosomal recessive, with brachy-syn-polydactyly
Reversed	1
HGVS	NC_000009.11:g.94488885G>A
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000007742.5,