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rs121908167

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs121908167(C;G)
Make rs121908167(G;G)
ReferenceGRCh38 38.1/141
Chromosome1
Position110064679
GeneALX3
is asnp
is mentioned by
dbSNPrs121908167
ebirs121908167
HLIrs121908167
Exacrs121908167
Varsomers121908167
Maprs121908167
PheGenIrs121908167
hapmaprs121908167
1000 genomesrs121908167
hgdprs121908167
ensemblrs121908167
gopubmedrs121908167
geneviewrs121908167
scholarrs121908167
googlers121908167
pharmgkbrs121908167
gwascentralrs121908167
openSNPrs121908167
23andMers121908167
23andMe allrs121908167
SNP Nexus

SNPshotrs121908167
SNPdbers121908167
MSV3drs121908167
GWAS Ctlgrs121908167
Max Magnitude0
OMIM606014
Desc
Variant0003
Relatedalso
ClinVar
Risk rs121908167(G;G)
Alt rs121908167(G;G)
Reference rs121908167(C;C)
Significance Pathogenic
Disease Frontonasal dysplasia 1
Variation info
Gene ALX3
CLNDBN Frontonasal dysplasia 1
Reversed 1
HGVS NC_000001.10:g.110607301G>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000004907.2,