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rs121908169

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs121908169(A;A)
Make rs121908169(A;T)
ReferenceGRCh38 38.1/141
Chromosome1
Position110064638
GeneALX3
is asnp
is mentioned by
dbSNPrs121908169
ebirs121908169
HLIrs121908169
Exacrs121908169
Varsomers121908169
Maprs121908169
PheGenIrs121908169
hapmaprs121908169
1000 genomesrs121908169
hgdprs121908169
ensemblrs121908169
gopubmedrs121908169
geneviewrs121908169
scholarrs121908169
googlers121908169
pharmgkbrs121908169
gwascentralrs121908169
openSNPrs121908169
23andMers121908169
23andMe allrs121908169
SNP Nexus

SNPshotrs121908169
SNPdbers121908169
MSV3drs121908169
GWAS Ctlgrs121908169
Max Magnitude0
OMIM606014
Desc
Variant0005
Relatedalso
ClinVar
Risk rs121908169(A;A)
Alt rs121908169(A;A)
Reference rs121908169(T;T)
Significance Pathogenic
Disease Frontonasal dysplasia 1
Variation info
Gene ALX3
CLNDBN Frontonasal dysplasia 1
Reversed 1
HGVS NC_000001.10:g.110607260A>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000004909.2,