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rs121908168

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs121908168(C;T)
Make rs121908168(T;T)
ReferenceGRCh38 38.1/141
Chromosome1
Position110064634
GeneALX3
is asnp
is mentioned by
dbSNPrs121908168
ebirs121908168
HLIrs121908168
Exacrs121908168
Varsomers121908168
Maprs121908168
PheGenIrs121908168
hapmaprs121908168
1000 genomesrs121908168
hgdprs121908168
ensemblrs121908168
gopubmedrs121908168
geneviewrs121908168
scholarrs121908168
googlers121908168
pharmgkbrs121908168
gwascentralrs121908168
openSNPrs121908168
23andMers121908168
23andMe allrs121908168
SNP Nexus

SNPshotrs121908168
SNPdbers121908168
MSV3drs121908168
GWAS Ctlgrs121908168
Max Magnitude0
OMIM606014
Desc
Variant0004
Relatedalso
ClinVar
Risk rs121908168(T;T)
Alt rs121908168(T;T)
Reference rs121908168(C;C)
Significance Pathogenic
Disease Frontonasal dysplasia 1
Variation info
Gene ALX3
CLNDBN Frontonasal dysplasia 1
Reversed 1
HGVS NC_000001.10:g.110607256G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000004908.2,