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rs876657391

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs876657391(-;-)
Make rs876657391(-;C)
ReferenceGRCh38.p2 38.2/147
Chromosome11
Position44275622
GeneALX4
is asnp
is mentioned by
dbSNPrs876657391
ebirs876657391
HLIrs876657391
Exacrs876657391
Varsomers876657391
Maprs876657391
PheGenIrs876657391
hapmaprs876657391
1000 genomesrs876657391
hgdprs876657391
ensemblrs876657391
gopubmedrs876657391
geneviewrs876657391
scholarrs876657391
googlers876657391
pharmgkbrs876657391
gwascentralrs876657391
openSNPrs876657391
23andMers876657391
23andMe allrs876657391
SNP Nexus

SNPshotrs876657391
SNPdbers876657391
MSV3drs876657391
GWAS Ctlgrs876657391
Max Magnitude0
ClinVar
Risk rs876657391(;)
Alt rs876657391(;)
Reference rs876657391(C;C)
Significance Pathogenic
Disease Frontonasal dysplasia 2
Variation info
Gene ALX4
CLNDBN Frontonasal dysplasia 2
Reversed 1
HGVS NC_000011.9:g.44297172delG
CLNSRC OMIM Allelic Variant
CLNACC RCV000170519.2,