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rs121909150

From SNPedia

Merged intors121909149
Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121909150(A;A)
Make rs121909150(A;G)
ReferenceGRCh38 38.1/141
Chromosome4
Position2831573
GeneSH3BP2
is asnp
is mentioned by
dbSNPrs121909150
ebirs121909150
HLIrs121909150
Exacrs121909150
Varsomers121909150
Maprs121909150
PheGenIrs121909150
hapmaprs121909150
1000 genomesrs121909150
hgdprs121909150
ensemblrs121909150
gopubmedrs121909150
geneviewrs121909150
scholarrs121909150
googlers121909150
pharmgkbrs121909150
gwascentralrs121909150
openSNPrs121909150
23andMers121909150
23andMe allrs121909150
SNP Nexus

SNPshotrs121909150
SNPdbers121909150
MSV3drs121909150
GWAS Ctlgrs121909150
StatusMerged into rs121909149
Max Magnitude0
OMIM602104
Desc
Variant0005
Relatedalso
ClinVar
Risk rs121909150(A;A)
Alt rs121909150(A;A)
Reference rs121909150(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
CLNSRC OMIM Allelic Variant
CLNACC SCV000028192.1,