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rs587777701

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
(G;G) 0 common in clinvar
Make rs587777701(C;G)
ReferenceGRCh38 38.1/142
Chromosome11
Position44275452
GeneALX4
is asnp
is mentioned by
dbSNPrs587777701
ebirs587777701
HLIrs587777701
Exacrs587777701
Varsomers587777701
Maprs587777701
PheGenIrs587777701
hapmaprs587777701
1000 genomesrs587777701
hgdprs587777701
ensemblrs587777701
gopubmedrs587777701
geneviewrs587777701
scholarrs587777701
googlers587777701
pharmgkbrs587777701
gwascentralrs587777701
openSNPrs587777701
23andMers587777701
23andMe allrs587777701
SNP Nexus

SNPshotrs587777701
SNPdbers587777701
MSV3drs587777701
GWAS Ctlgrs587777701
Max Magnitude0
ClinVar
Risk rs587777701(G;G)
Alt rs587777701(G;G)
Reference rs587777701(C;C)
Significance Pathogenic
Disease Frontonasal dysplasia 2
Variation info
Gene ALX4
CLNDBN Frontonasal dysplasia 2
Reversed 1
HGVS NC_000011.9:g.44297002G>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000144037.2,