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

rs587777847

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs587777847(-;-)
Make rs587777847(-;A)
ReferenceGRCh38 38.1/142
Chromosome1
Position243344302
GeneMIR4677, SDCCAG8
is asnp
is mentioned by
dbSNPrs587777847
ebirs587777847
HLIrs587777847
Exacrs587777847
Varsomers587777847
Maprs587777847
PheGenIrs587777847
hapmaprs587777847
1000 genomesrs587777847
hgdprs587777847
ensemblrs587777847
gopubmedrs587777847
geneviewrs587777847
scholarrs587777847
googlers587777847
pharmgkbrs587777847
gwascentralrs587777847
openSNPrs587777847
23andMers587777847
23andMe allrs587777847
SNP Nexus

SNPshotrs587777847
SNPdbers587777847
MSV3drs587777847
GWAS Ctlgrs587777847
Max Magnitude0
ClinVar
Risk rs587777847(;)
Alt rs587777847(;)
Reference rs587777847(A;A)
Significance Pathogenic
Disease Bardet-Biedl syndrome 16
Variation info
Gene SDCCAG8 MIR4677
CLNDBN Bardet-Biedl syndrome 16
Reversed 0
HGVS NC_000001.10:g.243507604delA
CLNSRC OMIM Allelic Variant
CLNACC RCV000144682.4,