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rs267606765

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs267606765(A;A)
Make rs267606765(A;G)
ReferenceGRCh38 38.1/141
Chromosome16
Position72012084
GeneDHODH
is asnp
is mentioned by
dbSNPrs267606765
ebirs267606765
HLIrs267606765
Exacrs267606765
Varsomers267606765
Maprs267606765
PheGenIrs267606765
hapmaprs267606765
1000 genomesrs267606765
hgdprs267606765
ensemblrs267606765
gopubmedrs267606765
geneviewrs267606765
scholarrs267606765
googlers267606765
pharmgkbrs267606765
gwascentralrs267606765
openSNPrs267606765
23andMers267606765
23andMe allrs267606765
SNP Nexus

SNPshotrs267606765
SNPdbers267606765
MSV3drs267606765
GWAS Ctlgrs267606765
Max Magnitude0
ClinVar
Risk rs267606765(A,C;A,C)
Alt rs267606765(A,C;A,C)
Reference rs267606765(G;G)
Significance Pathogenic
Disease Miller syndrome
Variation info
Gene DHODH
CLNDBN Miller syndrome
Reversed 0
HGVS NC_000016.9:g.72045983G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000018293.27,