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rs201915239

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs201915239(A;A)
Make rs201915239(A;G)
ReferenceGRCh38 38.1/142
Chromosome3
Position196487566
GeneRNF168
is asnp
is mentioned by
dbSNPrs201915239
ebirs201915239
HLIrs201915239
Exacrs201915239
Varsomers201915239
Maprs201915239
PheGenIrs201915239
hapmaprs201915239
1000 genomesrs201915239
hgdprs201915239
ensemblrs201915239
gopubmedrs201915239
geneviewrs201915239
scholarrs201915239
googlers201915239
pharmgkbrs201915239
gwascentralrs201915239
openSNPrs201915239
23andMers201915239
23andMe allrs201915239
SNP Nexus

SNPshotrs201915239
SNPdbers201915239
MSV3drs201915239
GWAS Ctlgrs201915239
Max Magnitude0
ClinVar
Risk rs201915239(A;A)
Alt rs201915239(A;A)
Reference rs201915239(G;G)
Significance Pathogenic
Disease Riddle syndrome
Variation info
Gene RNF168
CLNDBN Riddle syndrome
Reversed 0
HGVS NC_000003.11:g.196214437G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000128863.2,