Have questions? Visit https://www.reddit.com/r/SNPedia

rs387907146

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs387907146(C;T)
Make rs387907146(T;T)
ReferenceGRCh38 38.1/141
Chromosome16
Position4798631
GeneROGDI
is asnp
is mentioned by
dbSNPrs387907146
ebirs387907146
HLIrs387907146
Exacrs387907146
Varsomers387907146
Maprs387907146
PheGenIrs387907146
hapmaprs387907146
1000 genomesrs387907146
hgdprs387907146
ensemblrs387907146
gopubmedrs387907146
geneviewrs387907146
scholarrs387907146
googlers387907146
pharmgkbrs387907146
gwascentralrs387907146
openSNPrs387907146
23andMers387907146
23andMe allrs387907146
SNP Nexus

SNPshotrs387907146
SNPdbers387907146
MSV3drs387907146
GWAS Ctlgrs387907146
Max Magnitude0
ClinVar
Risk rs387907146(T;T)
Alt rs387907146(T;T)
Reference rs387907146(C;C)
Significance Pathogenic
Disease Kohlschutter's syndrome
Variation info
Gene ROGDI
CLNDBN Kohlschutter's syndrome
Reversed 1
HGVS NC_000016.9:g.4848632G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000024228.3,