Have questions? Visit https://www.reddit.com/r/SNPedia

rs104894122

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs104894122(A;A)
Make rs104894122(A;G)
ReferenceGRCh38 38.1/141
Chromosome9
Position91724248
GeneROR2
is asnp
is mentioned by
dbSNPrs104894122
ebirs104894122
HLIrs104894122
Exacrs104894122
Varsomers104894122
Maprs104894122
PheGenIrs104894122
hapmaprs104894122
1000 genomesrs104894122
hgdprs104894122
ensemblrs104894122
gopubmedrs104894122
geneviewrs104894122
scholarrs104894122
googlers104894122
pharmgkbrs104894122
gwascentralrs104894122
openSNPrs104894122
23andMers104894122
23andMe allrs104894122
SNP Nexus

SNPshotrs104894122
SNPdbers104894122
MSV3drs104894122
GWAS Ctlgrs104894122
Max Magnitude0
OMIM602337
Desc
Variant0002
Relatedalso
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,