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rs267606653

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs267606653(C;T)
Make rs267606653(T;T)
ReferenceGRCh38 38.1/141
Chromosome11
Position44267607
GeneALX4
is asnp
is mentioned by
dbSNPrs267606653
ebirs267606653
HLIrs267606653
Exacrs267606653
Varsomers267606653
Maprs267606653
PheGenIrs267606653
hapmaprs267606653
1000 genomesrs267606653
hgdprs267606653
ensemblrs267606653
gopubmedrs267606653
geneviewrs267606653
scholarrs267606653
googlers267606653
pharmgkbrs267606653
gwascentralrs267606653
openSNPrs267606653
23andMers267606653
23andMe allrs267606653
SNP Nexus

SNPshotrs267606653
SNPdbers267606653
MSV3drs267606653
GWAS Ctlgrs267606653
Max Magnitude0
ClinVar
Risk rs267606653(T;T)
Alt rs267606653(T;T)
Reference rs267606653(C;C)
Significance Pathogenic
Disease Frontonasal dysplasia 2
Variation info
Gene ALX4
CLNDBN Frontonasal dysplasia 2
Reversed 1
HGVS NC_000011.9:g.44289157G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000005323.3,