rs121909082

Orientation

minus

Stabilized

minus

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

Make rs121909082(A;A)

Make rs121909082(A;C)

Reference

GRCh38 38.1/141

Chromosome

9

Position

91724229

Gene

ROR2

is a	snp
is	mentioned by
dbSNP	rs121909082
dbSNP (classic)	rs121909082
ClinGen	rs121909082
ebi	rs121909082
HLI	rs121909082
Exac	rs121909082
Gnomad	rs121909082
Varsome	rs121909082
LitVar	rs121909082
Map	rs121909082
PheGenI	rs121909082
Biobank	rs121909082
1000 genomes	rs121909082
hgdp	rs121909082
ensembl	rs121909082
geneview	rs121909082
scholar	rs121909082
google	rs121909082
pharmgkb	rs121909082
gwascentral	rs121909082
openSNP	rs121909082
23andMe	rs121909082
SNPshot	rs121909082
SNPdbe	rs121909082
MSV3d	rs121909082
GWAS Ctlg	rs121909082

Max Magnitude

0

OMIM	602337
Desc
Variant	0001
Related	also

ClinVar
Risk	rs121909082(A;A) rs121909082(T;T)
Alt	rs121909082(A;A) rs121909082(T;T)
Reference	Rs121909082(C;C)
Significance	Pathogenic
Disease	Brachydactyly type B1
Variation	info
Gene	ROR2
CLNDBN	Brachydactyly type B1
Reversed	1
HGVS	NC_000009.11:g.94486511G>T
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000007727.3,