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rs1450425

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
(A;G) 0.5 benign most likely
(G;G) 0.5 benign most likely
ReferenceGRCh38.p2 38.2/144
Chromosome18
Position46529070
GeneLOXHD1
is asnp
is mentioned by
dbSNPrs1450425
ebirs1450425
HLIrs1450425
Exacrs1450425
Varsomers1450425
Maprs1450425
PheGenIrs1450425
hapmaprs1450425
1000 genomesrs1450425
hgdprs1450425
ensemblrs1450425
gopubmedrs1450425
geneviewrs1450425
scholarrs1450425
googlers1450425
pharmgkbrs1450425
gwascentralrs1450425
openSNPrs1450425
23andMers1450425
23andMe allrs1450425
SNP Nexus

SNPshotrs1450425
SNPdbers1450425
MSV3drs1450425
GWAS Ctlgrs1450425
Max Magnitude0.5
? (A;A) (A;G) (G;G) 28
ClinVar
Risk rs1450425(G;G)
Alt rs1450425(G;G)
Reference rs1450425(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene LOXHD1
CLNDBN not provided
Reversed 1
HGVS NC_000018.9:g.44109033T>C
CLNSRC
CLNACC RCV000171270.1,


[PMID 27242896] Fine-Mapping of 18q21.1 Locus Identifies Single Nucleotide Polymorphisms Associated with Nonsyndromic Cleft Lip with or without Cleft Palate.