rs104894121

Orientation

minus

Stabilized

minus

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

Make rs104894121(A;A)

Make rs104894121(A;G)

Reference

GRCh38 38.1/141

Chromosome

9

Position

91724247

Gene

ROR2

is a	snp
is	mentioned by
dbSNP	rs104894121
dbSNP (classic)	rs104894121
ClinGen	rs104894121
ebi	rs104894121
HLI	rs104894121
Exac	rs104894121
Gnomad	rs104894121
Varsome	rs104894121
LitVar	rs104894121
Map	rs104894121
PheGenI	rs104894121
Biobank	rs104894121
1000 genomes	rs104894121
hgdp	rs104894121
ensembl	rs104894121
geneview	rs104894121
scholar	rs104894121
google	rs104894121
pharmgkb	rs104894121
gwascentral	rs104894121
openSNP	rs104894121
23andMe	rs104894121
SNPshot	rs104894121
SNPdbe	rs104894121
MSV3d	rs104894121
GWAS Ctlg	rs104894121

Max Magnitude

0

OMIM	602337
Desc
Variant	0002
Related	also

ClinVar
Risk	rs104894121(A;A)
Alt	rs104894121(A;A)
Reference	Rs104894121(G;G)
Significance	Pathogenic
Disease	Brachydactyly type B1
Variation	info
Gene	ROR2
CLNDBN	Brachydactyly type B1
Reversed	1
HGVS	NC_000009.11:g.94486529C>T
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000007736.5,