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rs201938124

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs201938124(G;T)
Make rs201938124(T;T)
ReferenceGRCh38 38.1/142
Chromosome7
Position33367863
GeneBBS9
is asnp
is mentioned by
dbSNPrs201938124
ebirs201938124
HLIrs201938124
Exacrs201938124
Varsomers201938124
Maprs201938124
PheGenIrs201938124
hapmaprs201938124
1000 genomesrs201938124
hgdprs201938124
ensemblrs201938124
gopubmedrs201938124
geneviewrs201938124
scholarrs201938124
googlers201938124
pharmgkbrs201938124
gwascentralrs201938124
openSNPrs201938124
23andMers201938124
23andMe allrs201938124
SNP Nexus

SNPshotrs201938124
SNPdbers201938124
MSV3drs201938124
GWAS Ctlgrs201938124
Max Magnitude0
ClinVar
Risk rs201938124(A,C,T;A,C,T)
Alt rs201938124(A,C,T;A,C,T)
Reference rs201938124(G;G)
Significance Pathogenic
Disease Bardet-Biedl syndrome 9
Variation info
Gene BBS9
CLNDBN Bardet-Biedl syndrome 9
Reversed 0
HGVS NC_000007.13:g.33407475G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000002775.4,