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rs587776614

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs587776614(-;-)
Make rs587776614(-;A)
ReferenceGRCh38 38.1/142
Chromosome11
Position44275621
GeneALX4
is asnp
is mentioned by
dbSNPrs587776614
ebirs587776614
HLIrs587776614
Exacrs587776614
Varsomers587776614
Maprs587776614
PheGenIrs587776614
hapmaprs587776614
1000 genomesrs587776614
hgdprs587776614
ensemblrs587776614
gopubmedrs587776614
geneviewrs587776614
scholarrs587776614
googlers587776614
pharmgkbrs587776614
gwascentralrs587776614
openSNPrs587776614
23andMers587776614
23andMe allrs587776614
SNP Nexus

SNPshotrs587776614
SNPdbers587776614
MSV3drs587776614
GWAS Ctlgrs587776614
Max Magnitude0
ClinVar
Risk rs587776614(;)
Alt rs587776614(;)
Reference rs587776614(A;A)
Significance Pathogenic
Disease Parietal foramina 2
Variation info
Gene ALX4
CLNDBN Parietal foramina 2
Reversed 0
HGVS NC_000011.9:g.44297171delA
CLNSRC OMIM Allelic Variant
CLNACC RCV000005319.4,