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rs398122376

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs398122376(-;-)
Make rs398122376(-;AAAA)
Make rs398122376(AAAA;AAAA)
ReferenceGRCh38 38.1/141
Chromosome1
Position170719753
GenePRRX1
is asnp
is mentioned by
dbSNPrs398122376
ebirs398122376
HLIrs398122376
Exacrs398122376
Varsomers398122376
Maprs398122376
PheGenIrs398122376
hapmaprs398122376
1000 genomesrs398122376
hgdprs398122376
ensemblrs398122376
gopubmedrs398122376
geneviewrs398122376
scholarrs398122376
googlers398122376
pharmgkbrs398122376
gwascentralrs398122376
openSNPrs398122376
23andMers398122376
23andMe allrs398122376
SNP Nexus

SNPshotrs398122376
SNPdbers398122376
MSV3drs398122376
GWAS Ctlgrs398122376
Max Magnitude0
ClinVar
Risk rs398122376(AAAA;AAAA)
Alt rs398122376(AAAA;AAAA)
Reference rs398122376(;)
Significance Pathogenic
Disease Dysgnathia complex
Variation info
Gene PRRX1
CLNDBN Dysgnathia complex
Reversed 0
HGVS NC_000001.10:g.170688891_170688894dupAAAA
CLNSRC OMIM Allelic Variant
CLNACC RCV000043530.27,