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rs121908166

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs121908166(A;G)
Make rs121908166(G;G)
ReferenceGRCh38 38.1/141
Chromosome1
Position110061550
GeneALX3
is asnp
is mentioned by
dbSNPrs121908166
ebirs121908166
HLIrs121908166
Exacrs121908166
Varsomers121908166
Maprs121908166
PheGenIrs121908166
hapmaprs121908166
1000 genomesrs121908166
hgdprs121908166
ensemblrs121908166
gopubmedrs121908166
geneviewrs121908166
scholarrs121908166
googlers121908166
pharmgkbrs121908166
gwascentralrs121908166
openSNPrs121908166
23andMers121908166
23andMe allrs121908166
SNP Nexus

SNPshotrs121908166
SNPdbers121908166
MSV3drs121908166
GWAS Ctlgrs121908166
Max Magnitude0
OMIM606014
Desc
Variant0002
Relatedalso
ClinVar
Risk rs121908166(G;G)
Alt rs121908166(G;G)
Reference rs121908166(A;A)
Significance Pathogenic
Disease Frontonasal dysplasia 1
Variation info
Gene ALX3
CLNDBN Frontonasal dysplasia 1
Reversed 1
HGVS NC_000001.10:g.110604172T>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000004906.2,