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rs587776684

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587776684(A;A)
Make rs587776684(A;G)
ReferenceGRCh38 38.1/142
Chromosome12
Position85283877
GeneALX1
is asnp
is mentioned by
dbSNPrs587776684
ebirs587776684
HLIrs587776684
Exacrs587776684
Varsomers587776684
Maprs587776684
PheGenIrs587776684
hapmaprs587776684
1000 genomesrs587776684
hgdprs587776684
ensemblrs587776684
gopubmedrs587776684
geneviewrs587776684
scholarrs587776684
googlers587776684
pharmgkbrs587776684
gwascentralrs587776684
openSNPrs587776684
23andMers587776684
23andMe allrs587776684
SNP Nexus

SNPshotrs587776684
SNPdbers587776684
MSV3drs587776684
GWAS Ctlgrs587776684
Max Magnitude0
ClinVar
Risk rs587776684(A;A)
Alt rs587776684(A;A)
Reference rs587776684(G;G)
Significance Pathogenic
Disease Frontonasal dysplasia 3
Variation info
Gene ALX1
CLNDBN Frontonasal dysplasia 3
Reversed 0
HGVS NC_000012.11:g.85677655G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000008579.5,