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rs104894121

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs104894121(A;A)
Make rs104894121(A;G)
ReferenceGRCh38 38.1/141
Chromosome9
Position91724247
GeneROR2
is asnp
is mentioned by
dbSNPrs104894121
ebirs104894121
HLIrs104894121
Exacrs104894121
Varsomers104894121
Maprs104894121
PheGenIrs104894121
hapmaprs104894121
1000 genomesrs104894121
hgdprs104894121
ensemblrs104894121
gopubmedrs104894121
geneviewrs104894121
scholarrs104894121
googlers104894121
pharmgkbrs104894121
gwascentralrs104894121
openSNPrs104894121
23andMers104894121
23andMe allrs104894121
SNP Nexus

SNPshotrs104894121
SNPdbers104894121
MSV3drs104894121
GWAS Ctlgrs104894121
Max Magnitude0
OMIM602337
Desc
Variant0002
Relatedalso
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,