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rs398122375

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs398122375(-;-)
Make rs398122375(-;A)
ReferenceGRCh38 38.1/141
Chromosome1
Position170719753
GenePRRX1
is asnp
is mentioned by
dbSNPrs398122375
ebirs398122375
HLIrs398122375
Exacrs398122375
Varsomers398122375
Maprs398122375
PheGenIrs398122375
hapmaprs398122375
1000 genomesrs398122375
hgdprs398122375
ensemblrs398122375
gopubmedrs398122375
geneviewrs398122375
scholarrs398122375
googlers398122375
pharmgkbrs398122375
gwascentralrs398122375
openSNPrs398122375
23andMers398122375
23andMe allrs398122375
SNP Nexus

SNPshotrs398122375
SNPdbers398122375
MSV3drs398122375
GWAS Ctlgrs398122375
Max Magnitude0
ClinVar
Risk rs398122375(;)
Alt rs398122375(;)
Reference rs398122375(A;A)
Significance Pathogenic
Disease Dysgnathia complex
Variation info
Gene PRRX1
CLNDBN Dysgnathia complex
Reversed 0
HGVS NC_000001.10:g.170688894delA
CLNSRC OMIM Allelic Variant
CLNACC RCV000043529.21,