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rs587777700

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587777700(C;C)
Make rs587777700(C;G)
ReferenceGRCh38 38.1/142
Chromosome11
Position44275479
GeneALX4
is asnp
is mentioned by
dbSNPrs587777700
ebirs587777700
HLIrs587777700
Exacrs587777700
Varsomers587777700
Maprs587777700
PheGenIrs587777700
hapmaprs587777700
1000 genomesrs587777700
hgdprs587777700
ensemblrs587777700
gopubmedrs587777700
geneviewrs587777700
scholarrs587777700
googlers587777700
pharmgkbrs587777700
gwascentralrs587777700
openSNPrs587777700
23andMers587777700
23andMe allrs587777700
SNP Nexus

SNPshotrs587777700
SNPdbers587777700
MSV3drs587777700
GWAS Ctlgrs587777700
Max Magnitude0
ClinVar
Risk rs587777700(A,C;A,C)
Alt rs587777700(A,C;A,C)
Reference rs587777700(G;G)
Significance Pathogenic
Disease Parietal foramina 2
Variation info
Gene ALX4
CLNDBN Parietal foramina 2
Reversed 0
HGVS NC_000011.9:g.44297029G>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000144036.3,