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rs772340154

From SNPedia

Orientationplus
Geno Mag Summary
(CGCTGGCCCGCG;CGCTGGCCCGCG) 0 common in clinvar
Make rs772340154(-;-)
Make rs772340154(-;CGCTGGCCCGCG)
ReferenceGRCh38.p2 38.2/144
Chromosome16
Position4802507
GeneROGDI
is asnp
is mentioned by
dbSNPrs772340154
ebirs772340154
HLIrs772340154
Exacrs772340154
Varsomers772340154
Maprs772340154
PheGenIrs772340154
hapmaprs772340154
1000 genomesrs772340154
hgdprs772340154
ensemblrs772340154
gopubmedrs772340154
geneviewrs772340154
scholarrs772340154
googlers772340154
pharmgkbrs772340154
gwascentralrs772340154
openSNPrs772340154
23andMers772340154
23andMe allrs772340154
SNP Nexus

SNPshotrs772340154
SNPdbers772340154
MSV3drs772340154
GWAS Ctlgrs772340154
Max Magnitude0
ClinVar
Risk rs772340154(;)
Alt rs772340154(;)
Reference rs772340154(CGCTGGCCCGCG;CGCTGGCCCGCG)
Significance Pathogenic
Disease Kohlschutter's syndrome
Variation info
Gene ROGDI
CLNDBN Kohlschutter's syndrome
Reversed 0
HGVS NC_000016.9:g.4852508_4852519delCGCTGGCCCGCG
CLNSRC OMIM Allelic Variant
CLNACC RCV000034353.5,