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rs387906319

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(CTGA;CTGA) 0 common in clinvar
Make rs387906319(-;-)
Make rs387906319(-;CTGA)
ReferenceGRCh38 38.1/141
Chromosome1
Position110064600
GeneALX3
is asnp
is mentioned by
dbSNPrs387906319
ebirs387906319
HLIrs387906319
Exacrs387906319
Varsomers387906319
Maprs387906319
PheGenIrs387906319
hapmaprs387906319
1000 genomesrs387906319
hgdprs387906319
ensemblrs387906319
gopubmedrs387906319
geneviewrs387906319
scholarrs387906319
googlers387906319
pharmgkbrs387906319
gwascentralrs387906319
openSNPrs387906319
23andMers387906319
23andMe allrs387906319
SNP Nexus

SNPshotrs387906319
SNPdbers387906319
MSV3drs387906319
GWAS Ctlgrs387906319
Max Magnitude0
ClinVar
Risk rs387906319(;)
Alt rs387906319(;)
Reference rs387906319(CTGA;CTGA)
Significance Pathogenic
Disease Frontonasal dysplasia 1
Variation info
Gene ALX3
CLNDBN Frontonasal dysplasia 1
Reversed 1
HGVS NC_000001.10:g.110607222_110607225delTCAG
CLNSRC OMIM Allelic Variant
CLNACC RCV000004910.2,