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rs387906667

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs387906667(C;C)
Make rs387906667(C;T)
ReferenceGRCh38 38.1/141
Chromosome1
Position170719822
GenePRRX1
is asnp
is mentioned by
dbSNPrs387906667
ebirs387906667
HLIrs387906667
Exacrs387906667
Varsomers387906667
Maprs387906667
PheGenIrs387906667
hapmaprs387906667
1000 genomesrs387906667
hgdprs387906667
ensemblrs387906667
gopubmedrs387906667
geneviewrs387906667
scholarrs387906667
googlers387906667
pharmgkbrs387906667
gwascentralrs387906667
openSNPrs387906667
23andMers387906667
23andMe allrs387906667
SNP Nexus

SNPshotrs387906667
SNPdbers387906667
MSV3drs387906667
GWAS Ctlgrs387906667
Max Magnitude0
ClinVar
Risk rs387906667(C;C)
Alt rs387906667(C;C)
Reference rs387906667(T;T)
Significance Pathogenic
Disease Dysgnathia complex
Variation info
Gene PRRX1
CLNDBN Dysgnathia complex
Reversed 0
HGVS NC_000001.10:g.170688963T>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000022701.25,