rs104894122

Orientation

minus

Stabilized

minus

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

Make rs104894122(A;A)

Make rs104894122(A;G)

Reference

GRCh38 38.1/141

Chromosome

9

Position

91724248

Gene

ROR2

is a	snp
is	mentioned by
dbSNP	rs104894122
dbSNP (classic)	rs104894122
ClinGen	rs104894122
ebi	rs104894122
HLI	rs104894122
Exac	rs104894122
Gnomad	rs104894122
Varsome	rs104894122
LitVar	rs104894122
Map	rs104894122
PheGenI	rs104894122
Biobank	rs104894122
1000 genomes	rs104894122
hgdp	rs104894122
ensembl	rs104894122
geneview	rs104894122
scholar	rs104894122
google	rs104894122
pharmgkb	rs104894122
gwascentral	rs104894122
openSNP	rs104894122
23andMe	rs104894122
SNPshot	rs104894122
SNPdbe	rs104894122
MSV3d	rs104894122
GWAS Ctlg	rs104894122

Max Magnitude

0

OMIM	602337
Desc
Variant	0002
Related	also

ClinVar
Risk	rs104894122(A;A)
Alt	rs104894122(A;A)
Reference	Rs104894122(G;G)
Significance	Pathogenic
Disease	Brachydactyly type B1
Variation	info
Gene	ROR2
CLNDBN	Brachydactyly type B1
Reversed	1
HGVS	NC_000009.11:g.94486530C>T
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000007728.4,