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rs267606766

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs267606766(A;A)
Make rs267606766(A;G)
ReferenceGRCh38 38.1/141
Chromosome16
Position72017043
GeneDHODH
is asnp
is mentioned by
dbSNPrs267606766
ebirs267606766
HLIrs267606766
Exacrs267606766
Varsomers267606766
Maprs267606766
PheGenIrs267606766
hapmaprs267606766
1000 genomesrs267606766
hgdprs267606766
ensemblrs267606766
gopubmedrs267606766
geneviewrs267606766
scholarrs267606766
googlers267606766
pharmgkbrs267606766
gwascentralrs267606766
openSNPrs267606766
23andMers267606766
23andMe allrs267606766
SNP Nexus

SNPshotrs267606766
SNPdbers267606766
MSV3drs267606766
GWAS Ctlgrs267606766
Max Magnitude0
ClinVar
Risk rs267606766(A;A)
Alt rs267606766(A;A)
Reference rs267606766(G;G)
Significance Pathogenic
Disease Miller syndrome
Variation info
Gene DHODH
CLNDBN Miller syndrome
Reversed 0
HGVS NC_000016.9:g.72050942G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000018294.27,