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rs121918322

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121918322(A;A)
Make rs121918322(A;G)
ReferenceGRCh38 38.1/141
Chromosome13
Position21681060
GeneFGF9
is asnp
is mentioned by
dbSNPrs121918322
ebirs121918322
HLIrs121918322
Exacrs121918322
Varsomers121918322
Maprs121918322
PheGenIrs121918322
hapmaprs121918322
1000 genomesrs121918322
hgdprs121918322
ensemblrs121918322
gopubmedrs121918322
geneviewrs121918322
scholarrs121918322
googlers121918322
pharmgkbrs121918322
gwascentralrs121918322
openSNPrs121918322
23andMers121918322
23andMe allrs121918322
SNP Nexus

SNPshotrs121918322
SNPdbers121918322
MSV3drs121918322
GWAS Ctlgrs121918322
Max Magnitude0
OMIM600921
Desc
Variant0001
Relatedalso
ClinVar
Risk rs121918322(A;A)
Alt rs121918322(A;A)
Reference rs121918322(G;G)
Significance Pathogenic
Disease Multiple synostoses syndrome 3
Variation info
Gene FGF9
CLNDBN Multiple synostoses syndrome 3
Reversed 0
HGVS NC_000013.10:g.22255199G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000009242.3,