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rs869025279

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs869025279(-;-)
Make rs869025279(-;G)
ReferenceGRCh38.p2 38.2/147
Chromosome17
Position49973766
GeneDLX4
is asnp
is mentioned by
dbSNPrs869025279
ebirs869025279
HLIrs869025279
Exacrs869025279
Varsomers869025279
Maprs869025279
PheGenIrs869025279
hapmaprs869025279
1000 genomesrs869025279
hgdprs869025279
ensemblrs869025279
gopubmedrs869025279
geneviewrs869025279
scholarrs869025279
googlers869025279
pharmgkbrs869025279
gwascentralrs869025279
openSNPrs869025279
23andMers869025279
23andMe allrs869025279
SNP Nexus

SNPshotrs869025279
SNPdbers869025279
MSV3drs869025279
GWAS Ctlgrs869025279
Max Magnitude0
ClinVar
Risk rs869025279(;)
Alt rs869025279(;)
Reference rs869025279(G;G)
Significance Pathogenic
Disease Orofacial cleft 15
Variation info
Gene DLX4
CLNDBN Orofacial cleft 15
Reversed 0
HGVS NC_000017.10:g.48051130delG
CLNSRC OMIM Allelic Variant
CLNACC RCV000207311.1,