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rs587777846

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(AGAT;AGAT) 0 common in clinvar
Make rs587777846(-;-)
Make rs587777846(-;GATA)
Make rs587777846(GATA;GATA)
ReferenceGRCh38 38.1/142
Chromosome1
Position243415712
GeneSDCCAG8
is asnp
is mentioned by
dbSNPrs587777846
ebirs587777846
HLIrs587777846
Exacrs587777846
Varsomers587777846
Maprs587777846
PheGenIrs587777846
hapmaprs587777846
1000 genomesrs587777846
hgdprs587777846
ensemblrs587777846
gopubmedrs587777846
geneviewrs587777846
scholarrs587777846
googlers587777846
pharmgkbrs587777846
gwascentralrs587777846
openSNPrs587777846
23andMers587777846
23andMe allrs587777846
SNP Nexus

SNPshotrs587777846
SNPdbers587777846
MSV3drs587777846
GWAS Ctlgrs587777846
Max Magnitude0
ClinVar
Risk rs587777846(;)
Alt rs587777846(;)
Reference rs587777846(AGAT;AGAT)
Significance Pathogenic
Disease Bardet-Biedl syndrome 16
Variation info
Gene SDCCAG8
CLNDBN Bardet-Biedl syndrome 16
Reversed 0
HGVS NC_000001.10:g.243579014_243579017delGATA
CLNSRC OMIM Allelic Variant
CLNACC RCV000144681.4,