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

rs606231137

From SNPedia

Orientationplus
Geno Mag Summary
(AAAC;AAAC) 0 common in clinvar
Make rs606231137(-;-)
Make rs606231137(-;AACA)
Make rs606231137(AACA;AACA)
ReferenceGRCh38.p2 38.2/144
Chromosome7
Position33383753
GeneBBS9
is asnp
is mentioned by
dbSNPrs606231137
ebirs606231137
HLIrs606231137
Exacrs606231137
Varsomers606231137
Maprs606231137
PheGenIrs606231137
hapmaprs606231137
1000 genomesrs606231137
hgdprs606231137
ensemblrs606231137
gopubmedrs606231137
geneviewrs606231137
scholarrs606231137
googlers606231137
pharmgkbrs606231137
gwascentralrs606231137
openSNPrs606231137
23andMers606231137
23andMe allrs606231137
SNP Nexus

SNPshotrs606231137
SNPdbers606231137
MSV3drs606231137
GWAS Ctlgrs606231137
Max Magnitude0
ClinVar
Risk rs606231137(;)
Alt rs606231137(;)
Reference rs606231137(AAAC;AAAC)
Significance Pathogenic
Disease Bardet-Biedl syndrome 9
Variation info
Gene BBS9
CLNDBN Bardet-Biedl syndrome 9
Reversed 0
HGVS NC_000007.13:g.33423365_33423368delAACA
CLNSRC OMIM Allelic Variant
CLNACC RCV000002781.5,