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rs587776883

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs587776883(G;G)
Make rs587776883(G;T)
ReferenceGRCh38 38.1/142
Chromosome18
Position23001782
GeneRBBP8
is asnp
is mentioned by
dbSNPrs587776883
ebirs587776883
HLIrs587776883
Exacrs587776883
Varsomers587776883
Maprs587776883
PheGenIrs587776883
hapmaprs587776883
1000 genomesrs587776883
hgdprs587776883
ensemblrs587776883
gopubmedrs587776883
geneviewrs587776883
scholarrs587776883
googlers587776883
pharmgkbrs587776883
gwascentralrs587776883
openSNPrs587776883
23andMers587776883
23andMe allrs587776883
SNP Nexus

SNPshotrs587776883
SNPdbers587776883
MSV3drs587776883
GWAS Ctlgrs587776883
Max Magnitude0
ClinVar
Risk rs587776883(G;G)
Alt rs587776883(G;G)
Reference rs587776883(T;T)
Significance Pathogenic
Disease Seckel syndrome 2
Variation info
Gene RBBP8
CLNDBN Seckel syndrome 2
Reversed 0
HGVS NC_000018.9:g.20581745T>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000023361.3,