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rs121918281

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs121918281(C;G)
Make rs121918281(G;G)
ReferenceGRCh38 38.1/141
Chromosome11
Position44114224
GeneEXT2
is asnp
is mentioned by
dbSNPrs121918281
ebirs121918281
HLIrs121918281
Exacrs121918281
Varsomers121918281
Maprs121918281
PheGenIrs121918281
hapmaprs121918281
1000 genomesrs121918281
hgdprs121918281
ensemblrs121918281
gopubmedrs121918281
geneviewrs121918281
scholarrs121918281
googlers121918281
pharmgkbrs121918281
gwascentralrs121918281
openSNPrs121918281
23andMers121918281
23andMe allrs121918281
SNP Nexus

SNPshotrs121918281
SNPdbers121918281
MSV3drs121918281
GWAS Ctlgrs121918281
Max Magnitude0
OMIM608210
Desc
Variant0005
Relatedalso
ClinVar
Risk rs121918281(G;G)
Alt rs121918281(G;G)
Reference rs121918281(C;C)
Significance Pathogenic
Disease Multiple exostoses type 2
Variation info
Gene EXT2
CLNDBN Multiple exostoses type 2
Reversed 0
HGVS NC_000011.9:g.44135774C>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000002579.3,