rs863223291

Orientation

minus

Stabilized

minus

Geno	Mag	Summary
(ACAAGCT;ACAAGCT)	0	common in clinvar
(I;I)	0	common genotype

Make rs863223291(-;-)

Make rs863223291(-;ACAAGCT)

Reference

GRCh38.p2 38.2/146

Chromosome

9

Position

91724551

Gene

ROR2

is a	snp
is	mentioned by
dbSNP	rs863223291
dbSNP (classic)	rs863223291
ClinGen	rs863223291
ebi	rs863223291
HLI	rs863223291
Exac	rs863223291
Gnomad	rs863223291
Varsome	rs863223291
LitVar	rs863223291
Map	rs863223291
PheGenI	rs863223291
Biobank	rs863223291
1000 genomes	rs863223291
hgdp	rs863223291
ensembl	rs863223291
geneview	rs863223291
scholar	rs863223291
google	rs863223291
pharmgkb	rs863223291
gwascentral	rs863223291
openSNP	rs863223291
23andMe	rs863223291
SNPshot	rs863223291
SNPdbe	rs863223291
MSV3d	rs863223291
GWAS Ctlg	rs863223291

Max Magnitude

0

ClinVar
Risk	rs863223291(-;-)
Alt	rs863223291(-;-)
Reference	Rs863223291(ACAAGCT;ACAAGCT)
Significance	Pathogenic
Disease	Robinow syndrome
Variation	info
Gene	ROR2
CLNDBN	Robinow syndrome, autosomal recessive
Reversed	1
HGVS	NC_000009.11:g.94486833_94486839delAGCTTGT
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000007737.3,