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rs387906325

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(TGCAAGACGC;TGCAAGACGC) 0 common in clinvar
Make rs387906325(-;-)
Make rs387906325(-;TGCAAGACGC)
ReferenceGRCh38 38.1/141
Chromosome11
Position44309669
GeneALX4
is asnp
is mentioned by
dbSNPrs387906325
ebirs387906325
HLIrs387906325
Exacrs387906325
Varsomers387906325
Maprs387906325
PheGenIrs387906325
hapmaprs387906325
1000 genomesrs387906325
hgdprs387906325
ensemblrs387906325
gopubmedrs387906325
geneviewrs387906325
scholarrs387906325
googlers387906325
pharmgkbrs387906325
gwascentralrs387906325
openSNPrs387906325
23andMers387906325
23andMe allrs387906325
SNP Nexus

SNPshotrs387906325
SNPdbers387906325
MSV3drs387906325
GWAS Ctlgrs387906325
Max Magnitude0
ClinVar
Risk rs387906325(;)
Alt rs387906325(;)
Reference rs387906325(TGCAAGACGC;TGCAAGACGC)
Significance Pathogenic
Disease Parietal foramina 2
Variation info
Gene ALX4
CLNDBN Parietal foramina 2
Reversed 1
HGVS NC_000011.9:g.44331219_44331228delGCGTCTTGCA
CLNSRC OMIM Allelic Variant
CLNACC RCV000005322.5,