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rs121909149

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121909149(C;C)
Make rs121909149(C;G)
ReferenceGRCh38 38.1/141
Chromosome4
Position2831573
GeneSH3BP2
is asnp
is mentioned by
dbSNPrs121909149
ebirs121909149
HLIrs121909149
Exacrs121909149
Varsomers121909149
Maprs121909149
PheGenIrs121909149
hapmaprs121909149
1000 genomesrs121909149
hgdprs121909149
ensemblrs121909149
gopubmedrs121909149
geneviewrs121909149
scholarrs121909149
googlers121909149
pharmgkbrs121909149
gwascentralrs121909149
openSNPrs121909149
23andMers121909149
23andMe allrs121909149
SNP Nexus

SNPshotrs121909149
SNPdbers121909149
MSV3drs121909149
GWAS Ctlgrs121909149
Merged fromRs121909150
Max Magnitude0
OMIM602104
Desc
Variant0004
Relatedalso
ClinVar
Risk rs121909149(A,C;A,C)
Alt rs121909149(A,C;A,C)
Reference rs121909149(G;G)
Significance Pathogenic
Disease Fibrous dysplasia of jaw
Variation info
Gene SH3BP2
CLNDBN Fibrous dysplasia of jaw
Reversed 0
HGVS NC_000004.11:g.2833300G>A; NC_000004.11:g.2833300G>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000007987.2, RCV000007986.3,